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1,3-Benzenedicarboxylic acid, 5-cycloheptyl-2-hydroxy, dimethyl ester is a complex organic compound with the chemical formula C18H24O6. It is derived from 1,3-benzenedicarboxylic acid, which is a dicarboxylic acid with two carboxylic acid groups attached to a benzene ring. The 5-cycloheptyl-2-hydroxy group is a cycloheptane ring with a hydroxyl group at the 2-position, and the dimethyl ester indicates that the two carboxylic acid groups are esterified with two methyl groups. 1,3-Benzenedicarboxylic acid, 5-cycloheptyl-2-hydroxy-, dimethyl ester is characterized by its unique molecular structure, which includes a benzene ring, a cycloheptane ring, and ester groups. It is likely to be used in the synthesis of various pharmaceuticals, polymers, or other specialty chemicals due to its diverse functional groups and potential for further chemical reactions.

90253-20-6

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90253-20-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90253-20-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,5 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90253-20:
(7*9)+(6*0)+(5*2)+(4*5)+(3*3)+(2*2)+(1*0)=106
106 % 10 = 6
So 90253-20-6 is a valid CAS Registry Number.

90253-20-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 5-cycloheptyl-2-hydroxybenzene-1,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names 5-Cycloheptyl-2-hydroxy-1,3-benzoldicarbonsaeure-dimethylester

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:90253-20-6 SDS

90253-20-6Downstream Products

90253-20-6Relevant academic research and scientific papers

Syntheses with Aliphatic Dialdehydes, XXXVIII. - Synthesis and Properties of Cycloalkylmalonaldehydes

Reichardt, Christian,Ferwanah, Abdel-Rahman,Pressler, Wilfried,Yun, Kyeong-Yeol

, p. 649 - 679 (2007/10/02)

Vilsmeier formylation of cycloalkyl-substituted enol ethers (7,14a - c,23) yields the cycloalkylmalonaldehydes 1 - 5 for the first time.In solution 1 - 5 exist in the (E)-s-(E) enol form as vinylogous carboxylic acids.The reaction of 1 - 5 with suitable electrophiles and nucleophiles leads to cycloalkyl-substituted open-chain (29,30), carbocyclic (31) as well as heterocyclic compounds (32-40) with peculiar properties due to the presence of the lipophilic cycloalkyl group.

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