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3-CHLORO-5,5-DIMETHYL-2-CYCLOHEXEN-1-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17530-69-7

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17530-69-7 Usage

Synthesis Reference(s)

Tetrahedron Letters, 30, p. 3753, 1989 DOI: 10.1016/S0040-4039(01)80646-8

Check Digit Verification of cas no

The CAS Registry Mumber 17530-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,3 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17530-69:
(7*1)+(6*7)+(5*5)+(4*3)+(3*0)+(2*6)+(1*9)=107
107 % 10 = 7
So 17530-69-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H11ClO/c1-8(2)4-6(9)3-7(10)5-8/h3H,4-5H2,1-2H3

17530-69-7 Well-known Company Product Price

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  • Alfa Aesar

  • (A10728)  3-Chloro-5,5-dimethyl-2-cyclohexen-1-one, 96%   

  • 17530-69-7

  • 5g

  • 572.0CNY

  • Detail
  • Alfa Aesar

  • (A10728)  3-Chloro-5,5-dimethyl-2-cyclohexen-1-one, 96%   

  • 17530-69-7

  • 25g

  • 2435.0CNY

  • Detail
  • Alfa Aesar

  • (A10728)  3-Chloro-5,5-dimethyl-2-cyclohexen-1-one, 96%   

  • 17530-69-7

  • 100g

  • 7817.0CNY

  • Detail

17530-69-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-5,5-dimethylcyclohex-2-en-1-one

1.2 Other means of identification

Product number -
Other names 5,5-dimethyl-3-chloro-2-cyclohexenone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17530-69-7 SDS

17530-69-7Relevant articles and documents

NOVEL CYP17 INHIBITORS/ANTIANDROGENS

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Page/Page column 95; 96, (2015/01/07)

Compounds of formula (I), wherein R1 to R8 A, B, Z1 and Z2 are as defined in the claims and pharmaceutically acceptable salts and esters thereof are disclosed. The compounds of formula (I) possess utility as androgen receptor antagonists (inhibitors) and/or cytochrome P450 monooxygenase 17a-hydroxylase/17,20-lyase (CYP17) inhibitors. The compounds are useful as medicaments in the treatment of cancer, particularly prostate cancer, and other androgen dependent conditions and diseases where androgen antagonism is desired.

An approach toward the synthesis of PPAP natural product garsubellin A: Construction of the tricyclic core

Mehta, Goverdhan,Bera, Mrinal K.

, p. 1815 - 1821 (2013/03/13)

In a study directed toward the bioactive natural product garsubellin A, an expedient route to the bicyclo[3.3.1]nonan-9-one bearing tricyclic core, with a bridgehead anchored tetrahydrofuran ring, is delineated. The approach emanating from commercially av

COMPOUNDS FOR THE TREATMENT AND PREVENTION OF INFLUENZA

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Page/Page column 59, (2011/09/14)

A compound of formula (I) as well as pharmaceutically acceptable salt thereof, wherein R1 to R4 and Ar are as defined in description and in claims, can be used as a medicament.

COMPOUNDS FOR THE TREATMENT AND PREVENTION OF INFLUENZA

-

Page/Page column 58-59, (2011/09/14)

A compound of formula (I) as well as pharmaceutically acceptable salt thereof, wherein R1 to R4 and Ar are as defined in description and in claims, can be used as a medicament.

COMPOUNDS FOR THE TREATMENT AND PREVENTION OF INFLUENZA

-

Page/Page column 32-33, (2011/08/22)

A compound of formula (I) as well as pharmaceutically acceptable salt thereof, wherein R1 to R4 and Ar are as defined in description and in claims, can be used as a medicament.

NEW TETRAHYDROPYRAZOLO[3,4-C]ISOQUINOLIN-5-AMINE DERIVATIVES

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Page/Page column 14; 15, (2010/09/17)

New tetrahydropyrazolo[3,4-c]isoquinolin-5-amine derivatives having the chemical structure of formula (I) are disclosed; as well as process for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of the phosphodiesterase IV (PDE4).

Studies in aza-Claisen rearrangement: Synthesis of dimedone-annelated unusual heterocycles

Majumdar,Samanta

, p. 4955 - 4958 (2007/10/03)

A number of 3-N-(4′-aryloxybut-2′-ynyl)N-methyl amino-5,5-dimethyl cyclohex-2-enones are synthesized in 62-65% yield by refluxing 3-chloro-5,5-dimethyl cyclohex-2-enone with a number of 4-aryloxy-4-chlorobut-2-ynes in ethanol for 4 h. The amines are then

Chlorine substitution reactions using trichloroisocyanuric acid with triphenylphosphine

Hiegel,Ramirez,Barr

, p. 1415 - 1419 (2007/10/03)

Trichloroisocyanuric acid with triphenylphosphine in anhydrous acetonitrile will convert alcohols into alkyl halides, carboxylic acids into acid chlorides, 1,3-diketones into vinyl chlorides, and amides into nitriles.

2,3,6,7,8,9-hexahydro-8,8-dimethyl-5-phenyl-1H-1,4-benzodiazepin-6-one

Egg,Knauseder,Mayr,Schopf

, p. 655 - 657 (2007/10/02)

Several approaches for the synthesis of the title compound 1 were investigated. Treatment of the ethane-1,2-diamine derivative 2 with phosphoryl chloride afforded 3-chloro-5,5-dimethylcyclohex-2-enone (3) and 1-(5,5-dimethyl-3-oxocyclohex-1-enyl)-4,5-dihydro-2-phenylimidazole (4). The reaction of 2-benzoyldimedone (5) with an equimolar amount of ethane-1,2-diamine led to the 2:1 adduct 6, whereas with an excess of ethane-1,2-diamine, 4,5-dihydro-2-phenylimidazole (7) and dimedone were obtained. The synthesis of the title compound 1 was achieved by reacting 2-benzoyl-3-chloro-5,5-dimethylcyclohex-2-enone (8) with ethane-1,2-diamine.

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