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1,3-Cyclohexanedicarboxylic acid, monoethyl ester, (1S,3R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

227783-03-1

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227783-03-1 Usage

Physical state

Colorless liquid

Uses

a. Plasticizer in the manufacturing of various plastics and polymers
b. Improves flexibility and durability of plastics
c. Suitable for a wide range of applications

Additional applications

a. Solvent in chemical synthesis
b. Component in fragrance and flavor formulations

Versatility

Versatile chemical with various industrial uses

Check Digit Verification of cas no

The CAS Registry Mumber 227783-03-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,7,7,8 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 227783-03:
(8*2)+(7*2)+(6*7)+(5*7)+(4*8)+(3*3)+(2*0)+(1*3)=151
151 % 10 = 1
So 227783-03-1 is a valid CAS Registry Number.

227783-03-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,3S)-3-ethoxycarbonylcyclohexane-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1,3-Cyclohexanedicarboxylic acid,monoethyl ester,(1S,3R)

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:227783-03-1 SDS

227783-03-1Relevant academic research and scientific papers

Enzymatic desymmetrization of cis-1,3-cyclohexanedicarboxylic acid diesters

Boaz, Neil W.

, p. 813 - 816 (1999)

cis-1,3-Cyclohexanedicarboxylic acid (1,3-CHDA) monoesters were prepared in high overall yield and high enantiomeric purity using a three step process from cis/trans-1,3-CHDA. The asymmetry is induced by an enzymatic hydrolytic desymmetrization of a meso

Synthesis of potent and selective inhibitors of Candida albicans N-myristoyltransferase based on the benzothiazole structure

Yamazaki, Kazuo,Kaneko, Yasushi,Suwa, Kie,Ebara, Shinji,Nakazawa, Kyoko,Yasuno, Kazuhiro

, p. 2509 - 2522 (2007/10/03)

Two parallel synthetic methods using solid-supported reagents were established to examine the rapid optimization of weak hit compound 1. Several compounds showed high potency in the low nanomolar range against N-myristoyltransferase. The structure-activity relationship (SAR) and antifungal activities of a series of novel 2-aminobenzothiazole N-myristoyltransferase inhibitors are presented.

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