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1,2,2-Trimethyl-1,3-cyclopentanedicarboxylic acid dimethyl ester is a complex organic compound with the chemical formula C11H18O4. It is a white crystalline solid that is soluble in organic solvents. 1,2,2-Trimethyl-1,3-cyclopentanedicarboxylic acid dimethyl ester is derived from the cyclopentanedicarboxylic acid family, featuring a cyclopentane ring with three carbon substituents (two methyl groups and a carboxyl group) and two ester groups attached to the carboxyl groups. The dimethyl ester form indicates that the two carboxyl groups are each esterified with a methyl group, enhancing the compound's reactivity and solubility properties. It is used in various chemical syntheses, particularly in the production of pharmaceuticals and specialty chemicals, due to its unique structure and functional groups.

7282-27-1

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7282-27-1 Usage

Type of compound

Dimethyl ester derivative

Parent compound

1,2,2-Trimethyl-1,3-cyclopentanedicarboxylic acid

Common uses

a. Plasticizer in the production of polyvinyl chloride (PVC) and other polymers
b. Softening agent for increased flexibility and resistance to breaking
c. Production of adhesives and coatings

Known for

Stability and heat resistance

Health and environmental risks

Requires proper handling and management to avoid potential risks

Check Digit Verification of cas no

The CAS Registry Mumber 7282-27-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,8 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7282-27:
(6*7)+(5*2)+(4*8)+(3*2)+(2*2)+(1*7)=101
101 % 10 = 1
So 7282-27-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O4/c1-11(2)8(9(13)15-4)6-7-12(11,3)10(14)16-5/h8H,6-7H2,1-5H3

7282-27-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethyl camphorate

1.2 Other means of identification

Product number -
Other names Camphersaeure-semi-methylester

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:7282-27-1 SDS

7282-27-1Relevant academic research and scientific papers

BENZAMIDE IMIDAZOPYRAZINE BTK INHIBITORS

-

Page/Page column 77, (2016/07/27)

Provided are Bruton's Tyrosine Kinase (Btk) inhibitor compounds according to Formula I, pharmaceutically acceptable salts thereof, pharmaceutical compositions thereof, or their use in therapy.

TERTIARY ALCOHOL IMIDAZOPYRAZINE BTK INHIBITORS

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Page/Page column 57, (2016/08/03)

Provided are Bruton's Tyrosine Kinase (Btk) inhibitor compounds according to Formula (I), pharmaceutically acceptable salts thereof, pharmaceutical compositions thereof, or their use in therapy.

BIARYLETHER IMIDAZOPYRAZINE BTK INHIBITORS

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Page/Page column 59-60, (2016/07/27)

The present invention provides Bruton's Tyrosine Kinase (Btk) inhibitor compounds according to Formula (I), or pharmaceutically acceptable salts thereof, or to pharmaceutical compositions comprising these compounds and to their use in therapy. In particular, the present invention relates to the use of Btk inhibitor compounds of Formula (I) in the treatment of Btk mediated disorders.

Reaction de l'anhydride camphorique sur differents composes aromatiques (Friedel Crafts) I. Etude des isomeres structuraux et des stereoisomeres obtenus

Chevallet, Pierre,Orzalesi, Henri

, p. 217 - 226 (2007/10/02)

The study of the condensation reaction of camphoric anhydride with various aromatic compounds led us to examine initially the complete structure and stereochemistry of the ketones obtained with anisole and dimethoxy-benzene.The structure of the different

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