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125520-01-6

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125520-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125520-01-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,5,2 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 125520-01:
(8*1)+(7*2)+(6*5)+(5*5)+(4*2)+(3*0)+(2*0)+(1*1)=86
86 % 10 = 6
So 125520-01-6 is a valid CAS Registry Number.

125520-01-6SDS

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 ETHYL 6-DEOXY-1-THIO-2,3,4-TRI-O-ACETYL-α-L-MANNOPYRANOSIDE

1.2 Other means of identification

Product number -
Other names 1,2,3,4-tetrahydrocarbazole-6-carboxylic acid ethyl ester

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:125520-01-6 SDS

125520-01-6Downstream Products

125520-01-6Relevant articles and documents

Synthesis of the tetrasaccharide glycoside moiety of Solaradixine and rapid NMR-based structure verification using the program CASPER

Angles d'Ortoli, Thibault,Widmalm, G?ran

, p. 912 - 927 (2016)

The major glycoalkaloid in the roots of Solanum laciniatum is Solaradixine having the branched tetrasaccharide β-d-Glcp-(1→2)-β-d-Glcp-(1→3)[α-l-Rhap-(1→2)]-β-d-Galp linked to O3 of the steroidal alkaloid Solasodine. We herein describe the synthesis of th

Synthesis of benzaldehyde-functionalized LewisX trisaccharide analogs for glyco-SAM formation

Kopitzki, Sebastian,Dilmaghani, Karim Akbari,Thiem, Joachim

, p. 10621 - 10636 (2013)

LewisX (Lex) antigen based carbohydrate-carbohydrate interactions are mediated by complexation of metal ions. Although theoretical studies about the influence of participating hydroxyl groups in the Le x trisaccharide head group (Gal

The synthesis and biological evaluation of mycobacterial p-hydroxybenzoic acid derivatives (p-HBADs)

Bourke, Jean,Brereton, Corinna F.,Gordon, Stephen V.,Lavelle, Ed C.,Scanlan, Eoin M.

, p. 1114 - 1123 (2014/02/14)

Mycobacterium tuberculosis establishes chronic infection and causes disease through manipulation of the host's innate and adaptive immune response. The bacterial cell wall is highly complex and contains a rich variety of glycosylated compounds that are se

CARBOHYDRATE FUNCTIONALISED SURFACES

-

Paragraph 0200; 0206-0207, (2014/09/29)

Carbohydrates are biomolecules that are involved in a range of biological processes and play key roles in, for instance, host immune response and cellular adhesion. Accordingly, functionalisation of medical devices such as stents, valves, catheters, prostheses and other devices for in vivoimplantation with carbohydrates is an area in which considerable interest is developing. Disclosed herein are surfaces having carbohydrates immobilised thereon. The carbohydrate has a linker moiety covalently bound thereto and the linker moiety has a carbon atom that forms a covalent bond with an atom on the target surface. The carbon based bond is a strong, non-hydrolysable covalent bond. Diazonium salts are utilised to produce the functionalised surfaces and they are particularly advantageous as they result in non-toxic readily escapable by-products

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