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109282-37-3

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109282-37-3 Usage

General Description

The chemical compound (1R,4S,5R,6S)-1,4-dimethyl-7-oxabicyclo[2.2.1]heptane-5,6-dicarboxylic acid is a bicyclic organic compound that contains two carboxylic acid groups. It has a complex molecular structure, with two methyl groups and an oxygen atom incorporated into a bicyclic ring system. The compound displays a high degree of stereochemistry, with four chiral centers, denoted by the "R" and "S" configurations. (1R,4S,5R,6S)-1,4-dimethyl-7-oxabicyclo[2.2.1]heptane-5,6-dicarboxylic acid may have potential applications in organic synthesis and pharmaceutical research, due to its unique structure and potential reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 109282-37-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,2,8 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 109282-37:
(8*1)+(7*0)+(6*9)+(5*2)+(4*8)+(3*2)+(2*3)+(1*7)=123
123 % 10 = 3
So 109282-37-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O5/c1-9-3-4-10(2,15-9)6(8(13)14)5(9)7(11)12/h5-6H,3-4H2,1-2H3,(H,11,12)(H,13,14)/t5-,6+,9-,10+

109282-37-3SDS

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 (1R,2S,3R,4S)-1,4-dimethyl-7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 7-Oxabicyclo(2.2.1)heptane-2,3-dicarboxylic acid,1,4-dimethyl-,(endo,endo)

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:109282-37-3 SDS

109282-37-3Relevant articles and documents

Stereoselective Syntheses of 3-Acetyl-1,2-dimethyl-1-cyclopentanols. Syntheses of dl-Plinols A, B, and C

Imagawa, Takeshi,Matsuura, Kazuyuki,Murai, Nobuyuki,Akiyama, Tetsuo,Kawanisi, Mituyosi

, p. 3020 - 3022 (2007/10/02)

c- and t-3-Acetyl-1,c-2-dimethyl-r-1-cyclopentanols and c-3-acetyl-1,t-2-dimethyl-r-1-cyclopentanol are synthesized stereoselectively and dl-plinols A, B, and C are prepared therefrom.

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