CAS No.51911-82-1,4,8-dimethylnona-1,3,7-triene Suppliers

Shandong Hanjiang Chemical Co., Ltd.

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1,3,7-Nonatriene,4,8-dimethyl-

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4,8-dimethylnona-1,3,7-triene

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KAISA GROUP INC

1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer

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Henan Tianfu Chemical Co., Ltd.

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Antimex Chemical Limied

Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali

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We are committed to providing our customers with the best products and services at the most competitive prices.Appearance:white powder Storage:Room temperature with sealed well Package:according to the clients requirement Application:Use as primary a

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1,3,7-NONATRIENE,4,8-DIMETHYL-Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express

1,3,7-NONATRIENE,4,8-DIMETHYL-

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Henan Kanbei Chemical Co.,LTD

factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin

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Zibo Hangyu Biotechnology Development Co., Ltd

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Chungking Joyinchem Co., Ltd.

Joyinchem have been committed to chemical supply for several years and have built good cooperation records with multinational chemical corporations and importers from all over the world. Our services include:-Spot goods-Contract manufacturing-Custom

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Finetech Industry Limited

FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the 4,8-dimethylnona-1,3,7-triene, CAS:51911-82-1 with the most competitive price and the

4,8-dimethylnona-1,3,7-triene

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Nanjing Raymon Biotech Co., Ltd.

1,3,7-Nonatriene,4,8-dimethyl- Storage:Store in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/Pharmaceutical intermediates Transportation:By Sea,by Air,By courier like DHL or Fedx. Port:Shanghai/Sh

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Chemical Co.Ltd

1,3,7-Nonatriene,4,8-dimethyl-Appearance:Off white to slight yellow solid Storage:Stored in shaded, cool and dry places Package:1L 5L 10L 25L bottle Application:pharma intermediate Transportation:Handle with cares to avoid damaging the packages. Prot

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INTERNATIONAL LABORATORY LIMITED

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Annecis Limited

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Synthetic route

: 917-64-6
methyl magnesium iodide

: 5392-40-5
(E/Z)-3,7-dimethyl-2,6-octadienal

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

Conditions

Conditions	Yield
With diethyl ether erhitzt den erhaltenen Alkohol mit Essigsaeureanhydrid auf 120-130grad;

: 1779-49-3
Methyltriphenylphosphonium bromide

: 5392-40-5
(E/Z)-3,7-dimethyl-2,6-octadienal

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

Conditions

Conditions	Yield
(i) PhLi, Et2O, (ii) /BRN= 1721871/; Multistep reaction;

: 5988-79-4, 93354-31-5
3,6,6-trimethyl-(4at,8at)-hexahydro-3r,5c-ethano-pyrano[3,4-c]pyran-1,8-dione

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

Conditions

Conditions	Yield
copper at 190 - 210℃; for 8h;

: methylmagnesium iodide

: 5392-40-5
(E/Z)-3,7-dimethyl-2,6-octadienal

diluted acid: diluted acid

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

Conditions

Conditions	Yield
Wasserabspaltung aus dem primaer gebildeten Alkohol;

...Expand

: methyl magnesium (1+); bromide

: 5392-40-5
(E/Z)-3,7-dimethyl-2,6-octadienal

diluted acid: diluted acid

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

Conditions

Conditions	Yield
infolge Wasserabspaltung dem primaer gebildeten Alkohol;

...Expand

: pinacolboratamethylenetriphenylphosphonium iodide

: 5392-40-5
(E/Z)-3,7-dimethyl-2,6-octadienal

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

Conditions

Conditions	Yield
Stage #1: pinacolboratamethylenetriphenylphosphonium iodide With lithium hexamethyldisilazane In N,N,N,N,N,N-hexamethylphosphoric triamide at 0℃; for 2h; Stage #2: (E/Z)-3,7-dimethyl-2,6-octadienal In N,N,N,N,N,N-hexamethylphosphoric triamide at -78 - 20℃;	99 % Chromat.

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 28075-50-5
cyclohex-1-en-1-yl trifluoromethane sulfonate

: C17H28

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Reagent/catalyst; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	94%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 170011-47-9
1,4-dioxaspiro[4.5]dec-7-en-8-yl trifluoromethanesulfonate

: (E)-8-(4,8-dimethylnona-3,7-dien-2-yl)-1,4-dioxaspiro[4.5]dec-7-ene

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	88%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: C13H23F3O4SSi

: tert-butyl((3-((E)-4,8-dimethylnona-3,7-dien-2-yl)cyclohex-2-en-1-yl)oxy)dimethylsilane

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	85%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 606926-42-5
N-(4-methylphenylsulfonyl)-4-[(trifluoromethanesulfonyl)oxy]-1,2,3,6-tetrahydropyridine

: (E)-4-(4,8-dimethylnona-3,7-dien-2-yl)-1-tosyl-1,2,3,6-tetrahydropyridine

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	85%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: C9H13F3O5S

: (E)-6,8,12-trimethyl-5-methylenetrideca-7,11-dien-1-yl acetate

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	85%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 28075-49-2
1-cyclopentenyl triflate

: (E)-1-(4,8-dimethylnona-3,7-dien-2-yl)cyclopent-1-ene

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	83%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 188975-30-6
5,6-dihydro-4-trifluoromethylsulfonyloxy-2H-pyran

: (E)-4-(4,8-dimethylnona-3,7-dien-2-yl)-3,6-dihydro-2H-pyran

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	81%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 7-oxo-7-(p-tolylamino)hept-1-en-2-yl trifluoromethanesulfonate

: (E)-7,9,13-trimethyl-6-methylene-N-(p-tolyl)tetradeca-8,12-dienamide

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	80%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 77412-96-5
1-trifluoromethanesulfonyloxy-4-t-butylcyclohexene

: 4-(tert-butyl)-1-((E)-4,8-dimethylnona-3,7-dien-2-yl)cyclohex-1-ene

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	79%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: PhCH2CH2C(=CH2)OTf

: (E)-(4,6,10-trimethyl-3-methyleneundeca-5,9-dien-1-yl)benzene

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	79%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: methyl 6-(((trifluoromethyl)sulfonyl)oxy)hept-6-enoate

: C19H32O2

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	79%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: C23H24F4O5S

: (E)-7,9,13-trimethyl-6-methylenetetradeca-8,12-dien-1-yl 2-(2-fluoro-[1,1'-biphenyl]-4-yl)propanoate

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	74%

: 181180-42-7
3,6-dihydro-2H-thiopyran-4-enol trifluoromethanesulfonate

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: (E)-4-(4,8-dimethylnona-3,7-dien-2-yl)-3,6-dihydro-2H-thiopyran

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	72%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 122948-47-4
4-phenylcyclohex-1-enyl trifluoromethanesulfonate

: C23H32

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	72%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 122948-57-6
ethyl 4-(((trifluoromethyl)sulfonyl)oxy)cyclohex-3-enecarboxylate

: ethyl 4-((E)-4,8-dimethylnona-3,7-dien-2-yl)cyclohex-3-ene-1-carboxylate

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	71%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 123994-49-0
3,4-dihydro-1-naphthyl triflate

: 4-((E)-4,8-dimethylnona-3,7-dien-2-yl)-1,2,3,8a-tetrahydronaphthalene

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	71%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 28075-35-6
1-cyclooctenyl triflate

: (E)-1-(4,8-dimethylnona-3,7-dien-2-yl)cyclohept-1-ene

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	69%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: hept-1-en-2-yl trifluoromethanesulfonate

: (E)-2,6,8-trimethyl-9-methylenetetradeca-2,6-diene

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	63%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 28075-51-6
cyclohept-1-en-1-yl trifluoromethanesulfonate

: (E)-1-(4,8-dimethylnona-3,7-dien-2-yl)cyclohept-1-ene

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	62%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 7-hydroxyhept-1-en-2-yl trifluoromethanesulfonate

: (E)-6,8,12-trimethyl-5-methylenetrideca-7,11-dien-1-ol

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	62%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 109459-30-5
3-hydroxycyclohex-1-en-1-yl trifluoromethanesulfonate

: 3-((E )-4,8-dimethylnona-3,7-dien-2-yl)cyclohex-2-en-1-ol

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	60%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 1346777-33-0
(4R,4aS,6R)-4,4a-dimethyl-6-(prop-1-en-2-yl)-3,4,4a,5,6,7-hexahydronaphthalen-2-yl trifluoromethanesulfonate

: (2R,8R,8aS)-6-((E)-4,8-dimethylnona-3,7-dien-2-yl)-8,8a-dimethyl-2-(prop-1-en-2-yl)-1,2,3,7,8,8a-hexahydronaphthalene

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	53%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 58999-91-0, 58999-92-1
cyclododec-1-en-1-yl trifluoromethanesulfonate

: 1-(4,8-dimethylnona-3,7-dien-2-yl)cyclododec-1-ene

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	47%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 81827-59-0
Acetic acid (8R,9S,10R,13S,14S)-10,13-dimethyl-3-trifluoromethanesulfonyloxy-2,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl ester

: (8R,9S,10R,13S,14S)-3-((E)-4,8-dimethylnona-3,7-dien-2-yl)-10,13-dimethyl-2,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-ylacetate

Conditions

Conditions	Yield
With bis(1,5-cyclooctadiene)nickel(0); C35H46NP; cesium fluoride In tetrahydrofuran; di-isopropyl ether at 0℃; for 48h; Inert atmosphere; Sealed tube; Glovebox; regioselective reaction;	46%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 135747-07-8
methyl 2-diazo-3-oxo-3-(pyrrolidin-1-yl)propanoate

: 1198573-97-5
methyl 2-((E)-2,6-dimethylhepta-1,5-dienyl)-1-(pyrrolidin-1-ylcarbonyl)cyclopropanecarboxylate

Conditions

Conditions	Yield
With tetrakis[μ-(αS)-α-(1,1-dimethylethyl)-2,3-dihydro-1H-naphtho[1,8-cd]pyridine-2-acetato-κO:.kappaO']dirhodium(II)(Rh-Rh) In 1,2-dichloro-ethane at 25℃; for 16h; Inert atmosphere; optical yield given as %ee; enantioselective reaction;	45%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 99520-55-5
3-acetoxy-3-(4-methoxyphenyl)prop-1-yne

: (1E,4Z)-7-(4-methoxyphenyl)-6-methyl-6-(4-methylpent-3-enyl)cyclohepta-1,4-dienyl acetate

Conditions

Conditions	Yield
With [{(2-biphenyl)-di-tBu-phosphine}Au]SbF6 In 1,2-dichloro-ethane at 25 - 120℃; for 12.5h; Cope rearrangement; stereoselective reaction;	37%

: 51911-82-1
4,8-dimethyl-1,3,7-nonatriene

: 5-allyl-1,5-dimethyl-cyclohexene

Conditions

Conditions	Yield
With sulfuric acid

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