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877875-96-2

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877875-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 877875-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,7,8,7 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 877875-96:
(8*8)+(7*7)+(6*7)+(5*8)+(4*7)+(3*5)+(2*9)+(1*6)=262
262 % 10 = 2
So 877875-96-2 is a valid CAS Registry Number.

877875-96-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,2R)-1-(4-hydroxy-3-methoxyphenyl)-2-(4-((E)-3-hydroxyprop-1-en-1-yl)-2,6-dimethoxyphenoxy)propane-1,3-diol

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:877875-96-2 SDS

877875-96-2Downstream Products

877875-96-2Relevant articles and documents

Anti selective glycolate aldol reactions of (: S)-4-isopropyl-1-[(R)-1-phenylethyl]imidazolidin-2-one: application towards the asymmetric synthesis of 8-4′-oxyneolignans

Gangar, Mukesh,Ittuveetil, Avinash,Goyal, Sandeep,Pal, Anang,Harikrishnan,Nair, Vipin A.

, p. 102116 - 102126 (2016/11/09)

The anti selective glycolate aldol reactions of (S)-4-isopropyl-1-[(R)-1-phenylethyl]imidazolidin-2-one auxiliary have been standardized with high yields and excellent diastereoselectivities on various substituted aryl, allyl and alkyl aldehydes. The optimized reaction conditions were employed for the stereoselective synthesis of oxyneolignans.

Structure elucidation and NMR spectral assignments of four neolignan glycosides with enantiometric aglycones from Osmanthus ilicifolius

Machida, Koichi,Sakamoto, Shigeaki,Kikuchi, Masao

experimental part, p. 990 - 994 (2009/05/26)

Four new 8-O-4′ type neolignan glycosides with enantiometric aglycones, (7S,8R)-erythro-guaiacylglycerol-β-O-4′-sinapyl ether 9-O-β-D-glucopyranoside (1), (7R,8S)-erythro-guaiacylglycerol-β-O- 4′-sinapyl ether 9-O-β-D-glucopyranoside (2), (7S,8R)-erythro-

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