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107802-80-2

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  • Factory Price API 99% METHYL 2,3,4-TRI-O-BENZYL-1-THIO-BETA-L-FUCOPYRANOSIDE 107802-80-2 GMP Manufacturer

    Cas No: 107802-80-2

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107802-80-2 Usage

Chemical Properties

White to light yellow powder or crystal

Check Digit Verification of cas no

The CAS Registry Mumber 107802-80-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,8,0 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 107802-80:
(8*1)+(7*0)+(6*7)+(5*8)+(4*0)+(3*2)+(2*8)+(1*0)=112
112 % 10 = 2
So 107802-80-2 is a valid CAS Registry Number.
InChI:InChI=1/C28H32O4S/c1-21-25(29-18-22-12-6-3-7-13-22)26(30-19-23-14-8-4-9-15-23)27(28(32-21)33-2)31-20-24-16-10-5-11-17-24/h3-17,21,25-28H,18-20H2,1-2H3/t21-,25+,26+,27-,28+/m0/s1

107802-80-2 Well-known Company Product Price

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  • TCI America

  • (M1628)  Methyl 2,3,4-Tri-O-benzyl-1-thio-β-L-fucopyranoside  >95.0%(HPLC)

  • 107802-80-2

  • 1g

  • 2,320.00CNY

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107802-80-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3R,4R,5S,6R)-2-methyl-6-methylsulfanyl-3,4,5-tris(phenylmethoxy)oxane

1.2 Other means of identification

Product number -
Other names Methyl 2,3,4-tri-O-benzyl-b-L-thiofucopyranoside

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:107802-80-2 SDS

107802-80-2Downstream Products

107802-80-2Relevant articles and documents

New method for regioselective glycosylation employing saccharide oxyanions

Matwiejuk, Martin,Thiem, Joachim

experimental part, p. 5860 - 5878 (2011/11/06)

As an alternative concept for glycosylation, the prior activation of acceptor hydroxy groups for selective glycosidic bond formation, was investigated to give complex oligosaccharides. Oxyanions obtained from partially protected saccharides were glycosylated by employing glycopyranosyl halides, and the regiochemical results were studied. Initially, partially methylated methyl-α-D-glucopyranosides were used as a model system to study the underlying mechanistic principles of base-promoted glycosylation. High regioselectivities and stereospecific glycosidic bond formations were achieved, and the scope of the methodology was extended with different perbenzylated glycosyl donors.

Total synthesis of X hapten, III3 Fuc alpha-nLc4 Cer.

Sato,Ito,Nukada,Nakahara,Ogawa

, p. 197 - 210 (2007/10/02)

Total synthesis of O-beta-D-galactopyranosyl-(1----4)-O-[alpha-L- fucopyranosyl- (1----3)]-O-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-(1----3)-O-beta- D- galactopyranosyl- (1----4)-O-beta-D-glucopyranosyl-(1----1)-2-N-tetracosanoyl-(2S,3R ,4E)- sphinge

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