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4-[3,4-(METHYLENEDIOXY)PHENYL]-4-OXOBUTYRIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41764-07-2

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41764-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41764-07-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,7,6 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41764-07:
(7*4)+(6*1)+(5*7)+(4*6)+(3*4)+(2*0)+(1*7)=112
112 % 10 = 2
So 41764-07-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O5/c12-8(2-4-11(13)14)7-1-3-9-10(5-7)16-6-15-9/h1,3,5H,2,4,6H2,(H,13,14)

41764-07-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1,3-benzodioxol-5-yl)-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names CL 2684

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:41764-07-2 SDS

41764-07-2Relevant academic research and scientific papers

A highly stereocontrolled asymmetric total synthesis of epimer of (+)-7-deoxypancratistatin

Chavan, Subhash P.,Garai, Sumanta,Dey, Chandan,Gonnade, Rajesh G.

, p. 5562 - 5566 (2013/09/23)

A highly stereocontrolled asymmetric total synthesis of epimer of (+)-7-deoxypancratistatin has been achieved from readily available starting materials via unified strategy employing Sharpless asymmetric dihydroxylation, ring closing metathesis, Overman rearrangement, hydrogenolysis and Bischler-Napieralski reaction in 15 purification steps with 15% overall yield.

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