CAS No.7298-89-7,1,1-DIMETHYL-4-CHLORO-3,5-CYCLOHEXANEDIONE Suppliers,MSDS download

Dayang Chem (Hangzhou) Co.,Ltd.

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2-Chloro-5,5-dimethyl-1,3-cyclohexanedione

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TAIZHOU ZHENYU BIOTECHNOLOGY CO., LTD

Zhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed

1,1-DIMETHYL-4-CHLORO-3,5-CYCLOHEXANEDIONE

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Bluecrystal chem-union

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Chlorodimedone

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Antimex Chemical Limied

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Chlorodimedone

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Hangzhou Fandachem Co.,Ltd

2-CHLORO-5,5-DIMETHYL-1,3-CYCLOHEXANEDIONEAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express

2-CHLORO-5,5-DIMETHYL-1,3-CYCLOHEXANEDIONE

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ZHEJIANG JIUZHOU CHEM CO.,LTD

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1,1-DIMETHYL-4-CHLORO-3,5-CYCLOHEXANEDIONE

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Amadis Chemical Co., Ltd.

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2-Chloro-5,5-diMethyl-1,3-cyclohexanedione

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Hangzhou Share Chemical Co., Ltd

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2-Chloro-5,5-diMethyl-1,3-cyclohexanedione

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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 1,1-DIMETHYL-4-CHLORO-3,5-CYCLOHEXANEDIONE, CAS:7298-89-7 with the most competitive p

1,1-DIMETHYL-4-CHLORO-3,5-CYCLOHEXANEDIONE

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Debye Scientific

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2-Chloro-5,5-dimethyl-1,3-cyclohexanedione

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Chlorodimedone

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Synthetic route

: 126-81-8
dimedone

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate In dichloromethane	95%
With N-chloro-succinimide; toluene-4-sulfonic acid In dichloromethane at 0 - 20℃;	91%
With N-chloro-succinimide In various solvent(s) at 20℃; for 0.5h;	86%

: 126-81-8
dimedone

A: 7298-86-4
2,2-dichloro-5,5-dimethylcyclohexane-1,3-dione

B: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

Conditions

Conditions	Yield
With zinc chloride diethyl ether; iron(III)porphyrinate In dichloromethane for 0.5h;	A 20% B 74%
With sulfuryl dichloride In benzene at 25℃; for 18h;	A 66% B 26%
With potassium bromate; hydrogenchloride In N,N-dimethyl-formamide at 20℃; for 12h;	A 10% B 40%
With sodium hypochlorite; iron(III)porphyrinate; triethylbenzylammonium hypochlorite; acetic acid In dichloromethane for 0.5h; Product distribution; various iron(III)porphyrinate adducts, Lewis acids, various products and yields;

: 67-56-1
methanol

: 75-09-2
dichloromethane

: 1807-68-7
diazodimedone

A: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

B: 3-hydroxy-5,5-dimethyl-2-methoxy-2-cyclohexen-1-one

C: 2-chloro-3-(chloromethoxy)-5,5-dimethylcyclohex-2-en-1-one

Conditions

Conditions	Yield
dirhodium tetraacetate at 18 - 20℃; for 2h;	A 65% B 10% C 6%

...Expand

: 1807-68-7
diazodimedone

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

Conditions

Conditions	Yield
With dirhodium tetraacetate; dichloromethane; saccharin at 0 - 20℃;	61%

: 126-81-8
dimedone

A: 3359-52-2
bis(4,4-dimethyl-2,6-dioxo-1-cyclohexyl) sulfide

B: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

Conditions

Conditions	Yield
With SCl In benzene at 25℃; for 18h;	A 5% B 48%

: 126-81-8
dimedone

A: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

B: 83538-02-7
2-Hydroxydimedon

Conditions

Conditions	Yield
With 1H-imidazole; citrate-phosphate buffer; Mn-meso-tetrakis(3,5-disulphonatomesityl)porphyrinato; polyvinylpyridinium polymer (MnTMPS/PVP); dihydrogen peroxide; sodium chloride In water; acetonitrile for 1h; Product distribution; Ambient temperature; other reaction partner systems;	A 9% B 26%

: 7298-86-4
2,2-dichloro-5,5-dimethylcyclohexane-1,3-dione

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

Conditions

Conditions	Yield
With acid aqueous solution; potassium iodide
With hydrogenchloride; tin(ll) chloride
With sodium acetate In acetic acid Heating;
Multi-step reaction with 2 steps 1: HCl / dimethylformamide / 0.08 h / 160 - 165 °C 2: NaOAc / acetic acid / Heating View Scheme

: 7298-87-5
2-bromo-2-chloro-5,5-dimethylcyclohexane-1,3-dione

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

Conditions

Conditions	Yield
With potassium hydroxide; urea

: 17554-71-1
2,4-dichloro-5,5-dimethyl-cyclohexane-1,3-dione

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

Conditions

Conditions	Yield
With sodium acetate In acetic acid Heating;

: 126-81-8
dimedone

A: 17530-69-7
3-chloro-5,5-dimethylcyclohex-2-en-1-one

B: 56995-07-4
4',4',6,6-tetramethyl-6,7-dihydro-2'H,6'H-spiro[1,3-benzoxathiol-2,1'-cyclohexan]-2',4,6'(5H)-trion

C: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

D: C8H10Cl2O2S

Conditions

Conditions	Yield
With thionyl chloride In benzene Product distribution; Ambient temperature; investigation of effect of reaction times on product distribution;

...Expand

: 126-81-8
dimedone

A: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

B: 98593-03-4
2-iodo-5,5-dimethyl-1,3-cyclohexanedione

Conditions

Conditions	Yield
With styrene-co-(4-vinylpyridinium dichloroiodate) (1-) In acetic acid at 50℃; for 5h; Title compound not separated from byproducts;

: 35024-12-5
(4,4-dimethyl-2,6-dioxo-cyclohexyl)-phenyl-iodonium betaine

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

Conditions

Conditions	Yield
With acetyl chloride

: 33932-84-2
2--dimedon-betain

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

Conditions

Conditions	Yield
With hydrogenchloride Heating;

: 23383-02-0
Dimedon-(4-methoxy-phenyl)-iodonium-betain

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

Conditions

Conditions	Yield
With hydrogenchloride

: 14380-61-1
hypochlorite

: 126-81-8
dimedone

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

: 67-66-3
chloroform

: 126-81-8
dimedone

SeOCl2: SeOCl2

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

...Expand

: 7664-93-9
sulfuric acid

: 79255-35-9
2,3-dichloro-5,5-dimethylcyclohex-2-en-1-one

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

Conditions

Conditions	Yield
at 120℃;

: 7298-86-4
2,2-dichloro-5,5-dimethylcyclohexane-1,3-dione

KI: KI

acid solution: acid solution

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

...Expand

: 7647-01-0
hydrogenchloride

: 7298-86-4
2,2-dichloro-5,5-dimethylcyclohexane-1,3-dione

ethanolic solution: ethanolic solution

SnCl2: SnCl2

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

...Expand

: 7647-01-0
hydrogenchloride

: 7298-86-4
2,2-dichloro-5,5-dimethylcyclohexane-1,3-dione

tin dichloride: tin dichloride

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

...Expand

: 7298-87-5
2-bromo-2-chloro-5,5-dimethylcyclohexane-1,3-dione

: 57-13-6
urea

diluted KOH-solution: diluted KOH-solution

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

...Expand

: 3471-13-4
dimedone

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 2: AcCl View Scheme

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

: 3-bromo-2-chloro-5,5-dimethyl-2-cyclohexenone

Conditions

Conditions	Yield
With Oxalyl bromide In tetrahydrofuran at 0 - 20℃; for 2.5h;	94%
With oxalyl bromide In tetrahydrofuran at 0℃;

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

: 75-04-7
ethylamine

: 922-67-8
propynoic acid methyl ester

: methyl 1-ethyl-6,6-dimethyl-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylate

Conditions

Conditions	Yield
Stage #1: ethylamine; propynoic acid methyl ester With iron oxide In neat (no solvent) at 20℃; for 0.5h; Green chemistry; Stage #2: 2-chloro-5,5-dimethyl-1,3-cyclohexanedione In neat (no solvent) for 5h; Green chemistry;	87%

...Expand

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

: 488-17-5
3-methylbenzene-1,2-diol

: 7,8-dihydroxy-3,3,6-trimethyl-3,4-dihydrodibenzo[b,d]furan-1(2H)-one

Conditions

Conditions	Yield
With sodium acetate Michael addition; Electrochemical reaction;	81%

: 934-00-9
3-methocycatechol

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

: 7,8-dihydroxy-6-methoxy-3,3-dimethyl-3,4-dihydro-2H-dibenzofuran-1-one

Conditions

Conditions	Yield
With sodium acetate Michael addition; Electrochemical reaction;	80%

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

: 2393-23-9
4-methoxy-benzylamine

: 623-47-2
propynoic acid ethyl ester

: ethyl 1-(4-methoxybenzyl)-6,6-dimethyl-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylate

Conditions

Conditions	Yield
Stage #1: 4-methoxy-benzylamine; propynoic acid ethyl ester With iron oxide In neat (no solvent) at 20℃; for 0.5h; Green chemistry; Stage #2: 2-chloro-5,5-dimethyl-1,3-cyclohexanedione In neat (no solvent) for 5h; Green chemistry;	80%

...Expand

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

: 608-43-5
2,3-dimethyl-1,4-dihydroxybenzene

: 6,9-dihydroxy-3,3,7,8-tetramethyl-3,4-dihydro-2H-dibenzofuran-1-one

Conditions

Conditions	Yield
With sodium acetate Electrochemical reaction;	74%

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

: 7298-86-4
2,2-dichloro-5,5-dimethylcyclohexane-1,3-dione

Conditions

Conditions	Yield
With iron(III)porphyrinate; boron trifluoride diethyl etherate In dichloromethane for 0.5h;	73%
With sodium hypochlorite; iron(III)porphyrinate; triethylbenzylammonium hypochlorite; acetic acid In dichloromethane for 0.5h; Product distribution; various iron(III)porphyrinate adducts, Lewis acids, various products and yields;
With haloperoxidase from liverwort Bazzania trilobata; potassium chloride; dihydrogen peroxide In phosphate buffer
With vanadium-dependent haloperoxidase from the cyanobacterium Acaryochloris marina; potassium chloride; dihydrogen peroxide In aq. buffer at 30℃; pH=6; Enzymatic reaction;

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

: 7298-87-5
2-bromo-2-chloro-5,5-dimethylcyclohexane-1,3-dione

Conditions

Conditions	Yield
With tert.-butylhydroperoxide; Pyridine hydrobromide; VOL3(OEt) In chloroform-d1 at 20℃; for 24h;	70%
With chloroform; bromine
With water; bromine
With haloperoxidase from liverwort Bazzania trilobata; dihydrogen peroxide; potassium bromide In phosphate buffer
With vanadate-dependent bromoperoxidase II from Ascophyllum nodosum; dihydrogen peroxide; sodium sulfate; potassium bromide In aq. buffer at 22℃; pH=5.9; Kinetics; pH-value; Enzymatic reaction;

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

: 120-80-9
benzene-1,2-diol

: 63160-43-0
7,8-dihydroxy-3,3-dimethyl-3,4-dihydrodibenzo[b,d]furan-1(2H)-one

Conditions

Conditions	Yield
With sodium acetate Michael addition; Electrochemical reaction;	66%

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

A: 877-08-7
1,2,3,4-tetrachloro-5,6-dimethyl-benzene

B: 79255-35-9
2,3-dichloro-5,5-dimethylcyclohex-2-en-1-one

Conditions

Conditions	Yield
With chloroform; phosphorus pentachloride; phosphorus trichloride

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

: 22748-16-9
4,4-dimethylcyclopent-2-ene-1-one

Conditions

Conditions	Yield
With zinc(II) oxide at 220℃;

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

: 79255-35-9
2,3-dichloro-5,5-dimethylcyclohex-2-en-1-one

Conditions

Conditions	Yield
With chloroform; phosphorus pentachloride; phosphorus trichloride
With oxalyl dichloride In tetrahydrofuran at 0 - 20℃;

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

A: 79255-35-9
2,3-dichloro-5,5-dimethylcyclohex-2-en-1-one

B: 68266-68-2
1,2,3-trichloro-4,5-dimethyl-benzene

Conditions

Conditions	Yield
With chloroform; phosphorus pentachloride; phosphorus trichloride

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

: 146335-36-6
5-Chloro-2,3-dimethylphenol

Conditions

Conditions	Yield
With chloroform; phosphorus pentachloride

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

: 122-52-1
triethyl phosphite

: 80534-76-5
diethyl 5,5-dimethyl-3-oxocyclohex-1-enyl phosphate

Conditions

Conditions	Yield
With benzene

: 7298-89-7
2-chloro-5,5-dimethyl-1,3-cyclohexanedione

: 21428-78-4
4,6-Dibrom-2-chlor-dimedon

Conditions

Conditions	Yield
With hydrogen bromide; bromine In acetic acid

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Antimex Chemical Limied

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