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Phenyl 6-deoxy-3,4-bis-O-(phenylmethyl)-1-thio-alpha-L-mannopyranoside acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

636559-71-2

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636559-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 636559-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,6,5,5 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 636559-71:
(8*6)+(7*3)+(6*6)+(5*5)+(4*5)+(3*9)+(2*7)+(1*1)=192
192 % 10 = 2
So 636559-71-2 is a valid CAS Registry Number.

636559-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl 2-O-acetyl-3,4-di-O-benzyl-1-thio-α-L-rhamnopyranoside

1.2 Other means of identification

Product number -
Other names 1-S-PHENYL-2-O-ACETYL-3,4-DI-O-BENZYL-A-L-THIORHAMNOPYRANOSE

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:636559-71-2 SDS

636559-71-2Downstream Products

636559-71-2Relevant academic research and scientific papers

Synthetic Routes toward Acidic Pentasaccharide Related to the O-Antigen of E. coli 120 Using One-Pot Sequential Glycosylation Reactions

Mukherjee, Mana Mohan,Ghosh, Rina

supporting information, p. 5751 - 5760 (2017/06/07)

Concise syntheses of the acidic pentasaccharide, related to the O-antigenic polysaccharide of Escherichia coli 120, as its p-methoxyphenyl glycoside, have been achieved using a one-pot sequential glycosylation technique. The glycosylations have been accom

Efficient synthesis of O-antigen fragments expressed by Burkholderia anthina by modular synthesis approach

Nilsson, Inga,Michalik, Dirk,Silipo, Alba,Molinaro, Antonio,Vogel, Christian

, p. 98 - 107 (2015/03/05)

To facilitate mapping of the interaction region of the O-chain of the lipopolysaccharide from Burkholderia anthina and of a lipopolysaccharide-specific monoclonal antibody, trisaccharide propyl α-l-rhamnopyranosyl-(1→2)-α-d-galactopyranosyl-(1→3)-α-l-rham

RSK INHIBITORS AND THERAPEUTIC USES THEREOF

-

, (2008/06/13)

The present invention is directed to novel compounds and compositions that have Rsk specific inhibitory activity. In addition, inhibition of Rsk by the present compounds has been discovered to halt the proliferation of cancer cell lines while having little effect on the proliferation rate of normal cells. Therefore, the present invention identifies Rsk as a target for therapeutic intervention in diseased states in which the disease or the symptoms can be ameliorated by inhibition of Rsk catalytic activity.

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