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13225-19-9

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13225-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13225-19-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,2 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13225-19:
(7*1)+(6*3)+(5*2)+(4*2)+(3*5)+(2*1)+(1*9)=69
69 % 10 = 9
So 13225-19-9 is a valid CAS Registry Number.

13225-19-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2,3-di-O-benzyl-4,6-O-(R)-benzylidene-α-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names Methyl-4,6-di-O-benzylidene-2,3-di-O-benzyl-Alpha-D-glucopyranoside

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:13225-19-9 SDS

13225-19-9Relevant articles and documents

Substrate Substitution in Kanosamine Biosynthesis Using Phosphonates and Phosphite Rescue

Palmer, David R. J.,Vetter, Natasha D.

, p. 1926 - 1932 (2021/06/28)

Kanosamine is an antibiotic and antifungal compound synthesized from glucose 6-phosphate (G6P) inBacillus subtilisby the action of three enzymes: NtdC, which catalyzes NAD-dependent oxidation of the C3-hydroxyl; NtdA, a PLP-dependent aminotransferase; and

Triethylamine-methanol mediated selective removal of oxophenylacetyl ester in saccharides

Rasool, Javeed Ur,Kumar, Atul,Ali, Asif,Ahmed, Qazi Naveed

supporting information, p. 338 - 347 (2021/01/29)

A highly selective, mild, and efficient method for the cleavage of oxophenylacetyl ester protected saccharides was developed using triethylamine in methanol at room temperature. The reagent proved successful against different labile groups like acetal, ketal, and PMB and also generated good yields of the desired saccharides bearing lipid esters. Further, we also observed DBU in methanol as an alternative reagent for the deprotection of acetyl, benzoyl, and oxophenylacetyl ester groups. This journal is

How do Various Reaction Parameters Influence Anomeric Selectivity in Chemical Glycosylation with Thioglycosides and NIS/TfOH Activation?

Andersen, Sofie M.,Heuckendorff, Mads,Jensen, Henrik H.,Trinderup, Helle H.

, p. 3251 - 3259 (2021/06/25)

The reaction of glycosyl donor phenyl 2,3,4,6-tetra-O-benzyl-1-thio-β-D-glucopyranoside with NIS/TfOH(cat.) was systematically studied under various reaction conditions. Neither the molecular sieve pore size nor amount of NIS activator was found to have a

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