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135626-19-6

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135626-19-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135626-19-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,6,2 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 135626-19:
(8*1)+(7*3)+(6*5)+(5*6)+(4*2)+(3*6)+(2*1)+(1*9)=126
126 % 10 = 6
So 135626-19-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H12O5/c15-11(8-12-6-7-13(16)19-12)9-18-14(17)10-4-2-1-3-5-10/h1-8,11,15H,9H2/b12-8-/t11-/m0/s1

135626-19-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2S,3Z)-2-hydroxy-3-(5-oxofuran-2-ylidene)propyl] benzoate

1.2 Other means of identification

Product number -
Other names melodorinol

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:135626-19-6 SDS

135626-19-6Downstream Products

135626-19-6Relevant articles and documents

Total synthesis of (S)-(+)-melodorinol and (S)-(+)-acetylmelodorinol

Pohmakotr, Manat,Tuchinda, Patoomratana,Premkaisorn, Pornchai,Limpongpan, Attasit,Reutrakul, Vichai

, p. 795 - 802 (1999)

(S)-(+)-Melodorinol and (S)-(+)-acetylmelodorinol have been synthesized by reacting the lithiated butenolide with 2,3-O-alkylidene-D-glyceraldehyde followed by successive elimination, hydrolysis, benzoylation and acetylation reactions.

Total synthesis of acetylmelodorinol

Shen, Chien-Chang,Chou, Shiu-Ching,Chou, Cheng-Jen,Ho, Li-Kang

, p. 3141 - 3146 (1996)

An enantioselective total synthesis of bioactive melodorinol and acetylmelodorinol starting from 2,3-O-isopropylidene-D-glyceraldehyde and an alkoxyfuran is reported. Lithiation of the alkoxyfuran and subsequent reaction with the glyceraldehyde provided t

Total synthesis of both enantiomers of melodorinol. Redetermination of their absolute configurations

Lu, Xiyan,Chen, Guoying,Xia, Lijun,Guo, Guangzhong

, p. 3067 - 3072 (2007/10/03)

Both enantiomers of the natural products, melodorinol and acetylmelodorinol, have been synthesized by a palladium catalyzed enzyme coupling methodology. Their absolute configurations are redetermined.

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