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127062-02-6

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  • (4S,5R)-2,2,5-trimethyl-1,3-dioxolane-4-carboxylic acid

    Cas No: 127062-02-6

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127062-02-6 Usage

General Description

The chemical 1,3-Dioxolane-4-carboxylic acid, 2,2,5-trimethyl, (4S-trans)-(9CI) is a compound with the molecular formula C9H16O4 and a specific chemical structure. It is a carboxylic acid derivative with a dioxolane ring and three methyl groups attached to the carbon atoms. This chemical may be used in various industries, including pharmaceuticals, as a building block or intermediate in the synthesis of other compounds. Its exact properties, applications, and potential hazards should be further investigated and evaluated before any specific use.

Check Digit Verification of cas no

The CAS Registry Mumber 127062-02-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,0,6 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 127062-02:
(8*1)+(7*2)+(6*7)+(5*0)+(4*6)+(3*2)+(2*0)+(1*2)=96
96 % 10 = 6
So 127062-02-6 is a valid CAS Registry Number.

127062-02-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S,5R)-2,2,5-trimethyl-1,3-dioxolane-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:127062-02-6 SDS

127062-02-6Relevant articles and documents

Total synthesis of (-)-Jiadifenin

Yang, Yang,Fu, Xingnian,Chen, Jianwei,Zhai, Hongbin

, p. 9825 - 9828 (2012)

As easy as ABCD: (-)-Jiadifenin was synthesized in eighteen reaction steps from 1-[(E)-(4′-bromo-2′-butenyl)oxy]-4-methoxybenzene. Key features of this synthesis include: 1) Ireland-Claisen rearrangement to produce the two contiguous quaternary centers at

ENZYMATIC ENANTIOSELECTIVE HYDROLYSIS OF 2,2-DIMETHYL-1,3-DIOXOLANE-4-CARBOXYLIC ESTERS

Pottie, M.,Eycken, J. Van der,Vandewalle, M.,Dewanckele, J. M.,Roeper, H.

, p. 5319 - 5322 (2007/10/02)

2,2-dimethyl-1,3-dioxolane-4-carboxylic acid derived chiral building blocks were prepared from substituted α,β-unsaturated acids with high enantiomeric purities by enzymatic hydrolysis of their n.butyl esters.

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