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Dayang Chem (Hangzhou) Co.,Ltd.

DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe

Bicyclo[3.1.1]hept-2-ene-2-carboxaldehyde,6,6-dimethyl-

Cas:564-94-3

Min.Order:1 Kilogram

FOB Price: $3.0

Type:Lab/Research institutions

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Shanghai Upbio Tech Co.,Ltd

1.In No Less 10 years exporting experience. you can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specializ

Bicyclo[3.1.1]hept-2-ene-2-carboxaldehyde,6,6-dimethyl-

Cas:564-94-3

Min.Order:1 Gram

Negotiable

Type:Lab/Research institutions

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HANGZHOU YUNUO CHEMICAL CO.,LTD

superior quality moderate price & quick delivery Appearance:CLEAR COLOURLESS TO YELLOW LIQUID Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application

Bicyclo[3.1.1]hept-2-ene-2-carboxaldehyde,6,6-dimethyl-

Cas:564-94-3

Min.Order:1 Kilogram

Negotiable

Type:Trading Company

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Hangzhou J&H Chemical Co., Ltd.

J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia

Bicyclo[3.1.1]hept-2-ene-2-carboxaldehyde,6,6-dimethyl-

Cas:564-94-3

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

GIHI CHEMICALS CO.,LIMITED

Lower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe

(1R)-(-)-Myrtenal

Cas:564-94-3

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Henan Tianfu Chemical Co., Ltd.

Bicyclo[3.1.1]hept-2-ene-2-carboxaldehyde,6,6-dimethyl- Application:Organic Chemicals

564-94-3

Cas:564-94-3

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Antimex Chemical Limied

CSR1608-1755 Application:surface active agent

CSR1608-1755

Cas:564-94-3

Min.Order:0

Negotiable

Type:Lab/Research institutions

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Hangzhou Fandachem Co.,Ltd

Bicyclo[3.1.1]hept-2-ene-2-carboxaldehyde,6,6-dimethyl- cas 564-94-3Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express

Jilin haofei import and export trade Co.,Ltd

Price, service, company and transport advantage: 1. Best service, place of origin China, high quality, and reasonable price. 2. It's customers' right to choose the package (EMS, DHL, FEDEX, UPS). 3. It's customers' right

CSR1608-1755 CAS NO.564-94-3

Cas:564-94-3

Min.Order:0

Negotiable

Type:Trading Company

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Skyrun Industrial Co.,Ltd

Capacity, Prompt shipment Application:surface active agent

CSR1608-1755

Cas:564-94-3

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Changzhou Foreign Trade Corp

CFTC?PharmaChem?is?a?service?based?company?in?China,?a?pharmachem?division?of?Changzhou?Foreign?Trade?Corp.,supplying?raw?materials,?intermediates,?APIs?and?fine?chemicals?for?the?pharmaceutical?and?specialty?chemical?industries?worldwide. Applicatio

Pin-2-ene-1-carbaldehyde

Cas:564-94-3

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Synthetic route

myrtenol
515-00-4

myrtenol

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With bromobenzene; sodium hydride; triphenylphosphine; palladium diacetate In tetrahydrofuran at 65℃; for 1h;100%
With bromobenzene; sodium hydride; palladium diacetate; triphenylphosphine In tetrahydrofuran at 65℃; for 1h;95%
With calcium hydride; oxygen; 2,2,6,6-tetramethyl-piperidine-N-oxyl; copper dichloride In acetonitrile at 25℃; for 3h;93%
2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-[1,3]dioxolane

2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-[1,3]dioxolane

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With carbon tetrabromide In water; acetonitrile at 45℃; for 2h; sonication;99%
6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With pentafluorobenzeneseleninic acid In benzene for 2h; Heating;85%
With selenium(IV) oxide In 1,4-dioxane; ethanol at 60℃;70%
With perfluorooctylselenic acid; iodosylbenzene In various solvent(s) Heating;62%
With selenium(IV) oxide
With selenium(IV) oxide In 1,4-dioxane; ethanol at 65 - 95℃;

A

myrtenol
515-00-4

myrtenol

B

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With 2-(N-oxido)pyridineseleninic anhydride In dichloromethane at 20℃; for 18h;A 57%
B 28%
myrtenol
515-00-4

myrtenol

phenol
108-95-2

phenol

A

7,7-dimethyl-2-(hydroxymethyl)bicyclo<3.1.1>heptane
514-99-8

7,7-dimethyl-2-(hydroxymethyl)bicyclo<3.1.1>heptane

B

4-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-ylmethyl)phenol

4-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-ylmethyl)phenol

C

3-(2-((6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)methoxy)benzyl)-6,6-dimethylbicyclo[3.1.1]hept-2-ene

3-(2-((6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)methoxy)benzyl)-6,6-dimethylbicyclo[3.1.1]hept-2-ene

D

4-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-ylmethyl)-9-isopropyl-8,9,10,10a-tetrahydro-6H-benzo[c]chromene
1344744-38-2

4-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-ylmethyl)-9-isopropyl-8,9,10,10a-tetrahydro-6H-benzo[c]chromene

E

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
Stage #1: myrtenol; phenol With aluminum isopropoxide at 160℃;
Stage #2: With hydrogenchloride In water
A n/a
B 1.5%
C 12%
D n/a
E 6%
dichloromethane
75-09-2

dichloromethane

peroxyde de t-butyle et de myrtenyle
81971-91-7

peroxyde de t-butyle et de myrtenyle

3-dichloromethyl-2,10-epoxypinane

3-dichloromethyl-2,10-epoxypinane

B

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With sodium carbonate at 110℃; for 12h;A 10%
B 6%
Beta-pinene
177698-19-0

Beta-pinene

A

nopinone
24903-95-5

nopinone

B

pinocarvone
16812-40-1

pinocarvone

C

myrtenol
515-00-4

myrtenol

D

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With oxygen; titanium(IV) oxide In acetonitrile for 6h; Ambient temperature; Irradiation; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
Beta-pinene
177698-19-0

Beta-pinene

A

pinocarvone
16812-40-1

pinocarvone

B

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With oxygen; sodium acetate; sodium chloride; palladium dichloride 1.) AcOH, reflux; 2.) CH3CN, irradiation λ=366 nm; Yield given. Multistep reaction. Yields of byproduct given;
Beta-pinene
177698-19-0

Beta-pinene

A

myrtenyl hydroperoxide
58434-29-0

myrtenyl hydroperoxide

7,7-Dimethyl-3-oxatricyclo<4.1.1.02,4>octane-2-methanol
105815-51-8

7,7-Dimethyl-3-oxatricyclo<4.1.1.02,4>octane-2-methanol

C

myrtenol
515-00-4

myrtenol

D

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With oxygen; 5,15,10,20-tetraphenylporphyrin; Ti(O-t-Bu) In chloroform-d1 at 0℃; for 28h; Product distribution; Irradiation; other catalysts;A 43 % Spectr.
B 23 % Spectr.
C 16 % Spectr.
D 18 % Spectr.
With oxygen; 5,15,10,20-tetraphenylporphyrin; Ti(O-t-Bu) In chloroform-d1 at 0℃; for 28h; Irradiation;A 43 % Spectr.
B 23 % Spectr.
C 16 % Spectr.
D 18 % Spectr.

A

pinocarvone
16812-40-1

pinocarvone

6,6-Dimethylspirobicyclo<3.1.1>heptan-3-ol-2,2'-oxirane
33081-46-8

6,6-Dimethylspirobicyclo<3.1.1>heptan-3-ol-2,2'-oxirane

C

3-hydroxy-6,6-dimethylbicyclo[3.1.1]heptan-2-one
28664-04-2

3-hydroxy-6,6-dimethylbicyclo[3.1.1]heptan-2-one

D

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With oxygen; 5,15,10,20-tetraphenylporphyrin; titanium(IV) isopropylate In dichloromethane at 0℃; for 20h; Irradiation;A 5 % Spectr.
B 81 % Spectr.
C 9 % Spectr.
D 3 % Spectr.

A

pinocarvone
16812-40-1

pinocarvone

6,6-Dimethylspirobicyclo<3.1.1>heptan-3-ol-2,2'-oxirane
33081-46-8

6,6-Dimethylspirobicyclo<3.1.1>heptan-3-ol-2,2'-oxirane

C

3-hydroxy-6,6-dimethylbicyclo[3.1.1]heptan-2-one
28664-04-2

3-hydroxy-6,6-dimethylbicyclo[3.1.1]heptan-2-one

(1α,2β,4β,6α)-2,2,7-trimethyl-3-oxatricyclo[4.1.1.02,4]octane
32162-27-9

(1α,2β,4β,6α)-2,2,7-trimethyl-3-oxatricyclo[4.1.1.02,4]octane

E

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With oxygen; thiamine diphosphate; bis(acetylacetonate)oxovanadium In dichloromethane at 0℃; Product distribution; Irradiation; other catalysts;A 8 % Spectr.
B 46 % Spectr.
C 28 % Spectr.
D 10 % Spectr.
E 8 % Spectr.
myrtenyl hydroperoxide
58434-29-0

myrtenyl hydroperoxide

A

pinocarvone
16812-40-1

pinocarvone

C

myrtenol
515-00-4

myrtenol

D

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
In hexane at 40℃; for 3528h; Product distribution; isomerization reaction;

A

pinocarvone
16812-40-1

pinocarvone

C

myrtenyl hydroperoxide
58434-29-0

myrtenyl hydroperoxide

D

myrtenol
515-00-4

myrtenol

E

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With copper acetylacetonate Product distribution; Ambient temperature; other metal compounds; other hydroperoxide;
myrtenol
515-00-4

myrtenol

A

myrtenic acid
19250-17-0

myrtenic acid

B

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With chlorine dioxide In tetrachloromethane at 50℃; for 0.75h;A 4 % Chromat.
B 41 % Chromat.
dextrorotatory myrtenol

dextrorotatory myrtenol

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
d-myrtenal;
acetic acid
64-19-7

acetic acid

myrtenol
515-00-4

myrtenol

chromic acid

chromic acid

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

B

α-pinene epoxide
1686-14-2

α-pinene epoxide

C

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With 9,10-Dicyanoanthracene; oxygen In various solvent(s) Product distribution; Further Variations:; Reagents; Solvents; Oxidation; Irradiation;

C

α-pinene epoxide
1686-14-2

α-pinene epoxide

D

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With 9,10-Dicyanoanthracene; oxygen In acetonitrile Product distribution; Further Variations:; Solvents; Oxidation; Irradiation;
Beta-pinene
177698-19-0

Beta-pinene

A

pinocarvone
16812-40-1

pinocarvone

3-hydroxy-β-pinene
1674-08-4

3-hydroxy-β-pinene

C

myrtenol
515-00-4

myrtenol

D

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With oxygen; Co-Fe3O4 at 60℃; under 760.051 Torr; for 7h; Product distribution; Further Variations:; Catalysts;
Beta-pinene
177698-19-0

Beta-pinene

B

myrtenol
515-00-4

myrtenol

C

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With 2,6-dimethylpyridine; oxygen; rose bengal; acetic anhydride In methanol at 20℃; for 4h; UV-irradiation;
Beta-pinene
177698-19-0

Beta-pinene

A

myrtenol
515-00-4

myrtenol

B

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With oxygen; rose bengal In N,N-dimethyl-formamide at 20℃; for 4h; UV-irradiation;
Beta-pinene
177698-19-0

Beta-pinene

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With oxygen; rose bengal; acetic anhydride In methanol at 20℃; for 4h; UV-irradiation;
Conditions
ConditionsYield
With oxygen; rose bengal In N,N-dimethyl-formamide at 20℃; for 4h; UV-irradiation;
With dihydrogen peroxide In acetonitrile at 60℃; for 24h; Temperature;A 41 %Chromat.
B 13 %Chromat.
C 17 %Chromat.
D 11 %Chromat.
Conditions
ConditionsYield
With 2,6-dimethylpyridine; oxygen; rose bengal; acetic anhydride In methanol at 20℃; for 4h; UV-irradiation;
Beta-pinene
177698-19-0

Beta-pinene

A

pinocarvone
16812-40-1

pinocarvone

trans-pinocarveol

trans-pinocarveol

C

myrtenol
515-00-4

myrtenol

D

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With oxygen at 60℃; under 760.051 Torr; for 6h; Neat (no solvent);

A

verbenone
80-57-9

verbenone

C

pinocarvone
16812-40-1

pinocarvone

trans-pinocarveol

trans-pinocarveol

E

α-pinene epoxide
1686-14-2

α-pinene epoxide

F

myrtenol
515-00-4

myrtenol

G

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With oxygen at 60℃; under 760.051 Torr; for 6h; Neat (no solvent);

A

verbenone
80-57-9

verbenone

C

pinocarvone
16812-40-1

pinocarvone

trans-pinocarveol

trans-pinocarveol

E

myrtenol
515-00-4

myrtenol

F

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With oxygen at 60℃; under 3800.26 Torr; for 3.5h; Neat (no solvent); Autoclave;

A

pinocarvone
16812-40-1

pinocarvone

C

pinocarveyl hydroperoxide
22321-84-2

pinocarveyl hydroperoxide

D

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With 6,7-bis[3-(Nε-tert-butyloxycarbonyllysine methyl ester)]-1,3,5,8-tetramethyl-2,4-divinylporphyrin immobilized in silica gel In chloroform at 20℃; for 30h; Quantum yield; Time; Irradiation;

A

pinocarvone
16812-40-1

pinocarvone

trans-pinocarveol

trans-pinocarveol

C

pinocarveyl hydroperoxide
22321-84-2

pinocarveyl hydroperoxide

D

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

Conditions
ConditionsYield
With chlorophyll extract of fresh spinach leaves immobilized in silica gel In chloroform at 20℃; Reagent/catalyst; Irradiation;
(1S,2S)-1-phenyl-N2-methyl-1,2-propandiamine
130827-43-9

(1S,2S)-1-phenyl-N2-methyl-1,2-propandiamine

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

(1R,2R,3R,4S,5S)-2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-1,5-dimethyl-4-phenyl-imidazolidine
130827-39-3, 130857-87-3, 130857-92-0

(1R,2R,3R,4S,5S)-2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-1,5-dimethyl-4-phenyl-imidazolidine

Conditions
ConditionsYield
In chloroform for 24h; Ambient temperature;100%
1R,2S-N,N-dimethyl-2-phenyl-3-methyl-1,3-diaminoethane
130857-96-4

1R,2S-N,N-dimethyl-2-phenyl-3-methyl-1,3-diaminoethane

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

(1S,2S,3R,4S,5R)-2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-1,3,4-trimethyl-5-phenyl-imidazolidine
130827-41-7, 130857-89-5, 130857-95-3

(1S,2S,3R,4S,5R)-2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-1,3,4-trimethyl-5-phenyl-imidazolidine

Conditions
ConditionsYield
In chloroform for 24h; Ambient temperature;100%
6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

6,6-dimethylbicyclo<3.3.1>heptane-2-carboxaldehyde
4764-14-1

6,6-dimethylbicyclo<3.3.1>heptane-2-carboxaldehyde

Conditions
ConditionsYield
With hydrogen; SC-1 Ni2B In methanol at 25℃; under 760 Torr; for 24h;96%
With hydrido(triphenylphosphine)copper(I) hexamer; phenylsilane In toluene for 5h; Ambient temperature;80%
acetone
67-64-1

acetone

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

4-(6,6-dimethylbicyclo[3,1,1]hept-2-en-2-yl)-2-butanone
56933-99-4

4-(6,6-dimethylbicyclo[3,1,1]hept-2-en-2-yl)-2-butanone

Conditions
ConditionsYield
With Pd-MgO; hydrogen at 75℃; under 3750.38 Torr; for 3h;95%
6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

trimethyl orthoformate
149-73-5

trimethyl orthoformate

2,2-dimethoxymethyl-6,6-dimethyl-bicyclo[3.1.1]hept-2-ene
1263208-49-6

2,2-dimethoxymethyl-6,6-dimethyl-bicyclo[3.1.1]hept-2-ene

Conditions
ConditionsYield
With 1-ethyl-3-methylimidazolium hydrogensulfate In methanol at 5 - 20℃; for 2h;93%
1,3-cylohexanedione
504-02-9

1,3-cylohexanedione

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

C16H22O2

C16H22O2

Conditions
ConditionsYield
With ethylenediamine diacetic acid In neat (no solvent) at 20℃; for 0.5h; Knoevenagel Condensation; Green chemistry;93%
methylmagnesium chloride
676-58-4

methylmagnesium chloride

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

1-(6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-ethanol
33829-99-1

1-(6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-ethanol

Conditions
ConditionsYield
In tetrahydrofuran for 12h; Ambient temperature;92%
cyclopenta-1,3-diene
542-92-7

cyclopenta-1,3-diene

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

(1R)-(-)-myrtenal

(1R)-(-)-myrtenal

Conditions
ConditionsYield
With pyrrolidine In methanol for 5h; Inert atmosphere; Schlenk technique;90%
(1,3-dioxolan-2-yl-methyl)triphenylphosphonium bromide
52509-14-5

(1,3-dioxolan-2-yl-methyl)triphenylphosphonium bromide

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

(E)-3-(6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)prop-2-enal
124931-24-4

(E)-3-(6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)prop-2-enal

Conditions
ConditionsYield
Stage #1: (1,3-dioxolan-2-yl-methyl)triphenylphosphonium bromide With potassium tert-butylate In tetrahydrofuran at 0℃; for 0.5h; Sealed tube; Inert atmosphere;
Stage #2: 6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde In tetrahydrofuran at 20℃; for 6h; Sealed tube; Inert atmosphere;
90%
6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

myrtenol
515-00-4

myrtenol

Conditions
ConditionsYield
With lithium pyrrolidinoborohydride at 25℃;89%
With LiPyrrBH3 In tetrahydrofuran at 25℃; for 3h;89%
With sodium triphenyl boronhydride In tetrahydrofuran at 0℃; for 1h;100 % Chromat.
With formic acid; iron(II) tetrafluoroborate hexahydrate; tris(2-diphenylphosphinoethyl)phosphine In tetrahydrofuran at 60℃; for 2h; Schlenk technique; Inert atmosphere;99 %Chromat.
6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

α-pinenyl bromide
22339-11-3

α-pinenyl bromide

Conditions
ConditionsYield
Stage #1: 6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde With sodium tetrahydroborate In tetrahydrofuran at 20℃; for 8h;
Stage #2: With carbon tetrabromide; triphenylphosphine In tetrahydrofuran; dichloromethane at 0℃; for 0.5h;
84%
3,5-dimethyl-4-nitroisoxazole
1123-49-5

3,5-dimethyl-4-nitroisoxazole

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

5-[2-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)vinyl]-3-methyl-4-nitroisoxazole

5-[2-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)vinyl]-3-methyl-4-nitroisoxazole

Conditions
ConditionsYield
With piperidine In ethanol at 65℃; for 2h;81%
(Z)-2-cyano-3-mercapto-3-(phenylamino)acrylamide

(Z)-2-cyano-3-mercapto-3-(phenylamino)acrylamide

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

(RR,RS)-5-cyano-2-(6',6'-dimethylbicyclo[3.1.1]hept-2'-en-2'-yl)-6-phenylamino-2,3-dihydro-1,3-thiazin-4(1H)-one
884536-72-5

(RR,RS)-5-cyano-2-(6',6'-dimethylbicyclo[3.1.1]hept-2'-en-2'-yl)-6-phenylamino-2,3-dihydro-1,3-thiazin-4(1H)-one

Conditions
ConditionsYield
With toluene-4-sulfonic acid In ethanol for 2h; Heating;80%
4-methylthiosemicarbazide
6610-29-3

4-methylthiosemicarbazide

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

C12H19N3S

C12H19N3S

Conditions
ConditionsYield
With hydrogenchloride In ethanol at 85℃;80%
2,4-imidazolidinedione
461-72-3

2,4-imidazolidinedione

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

5-[1-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-meth-(Z)-ylidene]-imidazolidine-2,4-dione

5-[1-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-meth-(Z)-ylidene]-imidazolidine-2,4-dione

Conditions
ConditionsYield
With sodium acetate on alumina for 0.0333333h; microwave irradiation;76%
acetonitrile
75-05-8

acetonitrile

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

C12H17NO
324538-16-1

C12H17NO

Conditions
ConditionsYield
With [2,6-(iPr2PO)2C6H3]NiCH2CN at 20℃; for 24h; Inert atmosphere;73%
(1R,2S)-1-phenyl-N2-methyl-1,2-propandiamine
130827-42-8

(1R,2S)-1-phenyl-N2-methyl-1,2-propandiamine

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

A

(1R,2R,3S,4R,5S)-2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-1,5-dimethyl-4-phenyl-imidazolidine
130827-39-3, 130857-87-3, 130857-92-0

(1R,2R,3S,4R,5S)-2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-1,5-dimethyl-4-phenyl-imidazolidine

B

(1S,2S,3S,4R,5S)-2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-1,5-dimethyl-4-phenyl-imidazolidine
130827-39-3, 130857-87-3, 130857-92-0

(1S,2S,3S,4R,5S)-2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-1,5-dimethyl-4-phenyl-imidazolidine

Conditions
ConditionsYield
In chloroform for 24h; Ambient temperature;A 71%
B 12%
N-aminophthalamide
1875-48-5

N-aminophthalamide

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

A

2,3-dihydrophthalazine-1,4-dione
1445-69-8

2,3-dihydrophthalazine-1,4-dione

B

myrtenal phthaloylhydrazone
121597-24-8

myrtenal phthaloylhydrazone

Conditions
ConditionsYield
In ethanol for 2.5h; Heating;A n/a
B 67%
formic acid
64-18-6

formic acid

Cyclohexyl isocyanide
931-53-3

Cyclohexyl isocyanide

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

2-(cyclohexylamino)-1-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)-2-oxoethyl formate

2-(cyclohexylamino)-1-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)-2-oxoethyl formate

Conditions
ConditionsYield
In dichloromethane at 0 - 20℃; for 48h; Passerini Condensation; Inert atmosphere;66%
formic acid
64-18-6

formic acid

tert-butylisonitrile
119072-55-8, 7188-38-7

tert-butylisonitrile

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

2-(tert-butylamino)-1-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)-2-oxoethyl formate

2-(tert-butylamino)-1-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)-2-oxoethyl formate

Conditions
ConditionsYield
In dichloromethane at 0 - 20℃; for 48h; Passerini Condensation; Inert atmosphere;64%
N-Boc-(tri-n-butylstannyl)dimethylamine

N-Boc-(tri-n-butylstannyl)dimethylamine

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

1,1-dimethylethyl N-methyl-N-[(bicyclo[3.3.1](4,4-dimethyl-6-formyl)heptyl)methyl] carbamate

1,1-dimethylethyl N-methyl-N-[(bicyclo[3.3.1](4,4-dimethyl-6-formyl)heptyl)methyl] carbamate

Conditions
ConditionsYield
Stage #1: N-Boc-(tri-n-butylstannyl)dimethylamine With n-butyllithium In tetrahydrofuran at -78℃; for 0.283333h; Metallation;
Stage #2: In tetrahydrofuran at -78 - -53℃; for 0.416667h; Transmetallation;
Stage #3: 6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde With chloro-trimethyl-silane In tetrahydrofuran at -78 - 20℃; Substitution;
62%
(1S,2S)-1-phenyl-N1,N2-dimethyl-1,2-propandiamine
130857-97-5

(1S,2S)-1-phenyl-N1,N2-dimethyl-1,2-propandiamine

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

A

(1R,2R,3R,4S,5S)-2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-1,3,4-trimethyl-5-phenyl-imidazolidine
130827-41-7, 130857-89-5, 130857-95-3

(1R,2R,3R,4S,5S)-2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-1,3,4-trimethyl-5-phenyl-imidazolidine

B

(1R,2S,3R,4S,5S)-2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-1,3,4-trimethyl-5-phenyl-imidazolidine
130827-41-7, 130857-89-5, 130857-95-3

(1R,2S,3R,4S,5S)-2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-1,3,4-trimethyl-5-phenyl-imidazolidine

Conditions
ConditionsYield
In chloroform for 24h; Ambient temperature;A 60%
B 40%
1.3-propanedithiol
109-80-8

1.3-propanedithiol

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

2-(6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-[1,3]dithiane
69460-06-6

2-(6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-yl)-[1,3]dithiane

Conditions
ConditionsYield
With TAFF In benzene for 3h; Heating;60%
(S)-5-oxopyrrolidine-2-carbohydrazide
934-06-5

(S)-5-oxopyrrolidine-2-carbohydrazide

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

N'-((6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)methylene)-5-oxopyrrolidine-2-carbohydrazide

N'-((6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)methylene)-5-oxopyrrolidine-2-carbohydrazide

Conditions
ConditionsYield
With hydrazine hydrate In water at 20℃; for 1h;60%
formic acid
64-18-6

formic acid

p-chlorobenzylisocyanide
39546-47-9

p-chlorobenzylisocyanide

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

2-(4-chlorobenzylamino)-1-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)-2-oxoethyl formate

2-(4-chlorobenzylamino)-1-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)-2-oxoethyl formate

Conditions
ConditionsYield
In dichloromethane at 0 - 20℃; for 48h; Passerini Condensation; Inert atmosphere;57%
6,7-dimethoxy-1-cyanomethylene-1,2,3,4-tetrahydroisoquinoline
51054-41-2

6,7-dimethoxy-1-cyanomethylene-1,2,3,4-tetrahydroisoquinoline

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
564-94-3

6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde

C22H24N2O2

C22H24N2O2

Conditions
ConditionsYield
With cerium(III) chloride In acetonitrile at 20℃; for 6h;52%

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