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74162-08-6

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74162-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74162-08-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,6 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 74162-08:
(7*7)+(6*4)+(5*1)+(4*6)+(3*2)+(2*0)+(1*8)=116
116 % 10 = 6
So 74162-08-6 is a valid CAS Registry Number.

74162-08-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-di-O-Ac-MeXylp

1.2 Other means of identification

Product number -
Other names methyl 2,4-di-O-acetyl-β-D-xylopyranoside

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:74162-08-6 SDS

74162-08-6Relevant articles and documents

Positional specificity of Flavobacterium johnsoniae acetylxylan esterase and acetyl group migration on xylan main chain

Puchart, Vladimír,Gjermansen, Morten,Mastihubová, Mária,M?rkeberg Krogh, Kristian B.R.,Biely, Peter

, (2020/01/09)

A new Flavovacterium johnsoniae isolate encodes an enzyme that is essentially identical with a recently discovered novel acetylxylan esterase, capable of liberating 3-O-acetyl group from 4-O-methyl-D-glucuronic acid-substituted xylopyranosyl (Xylp) residues (Razeq et al., 2018). In addition to deesterification of the 2-O-MeGlcA-substituted Xylp residues in acetylglucuronoxylan, the enzyme acts equally well on doubly acetylated Xylp residues from which it liberates only the 3-O-acetyl groups, leaving the 2-O-acetyl groups untouched. 3-O-Monoacetylated Xylp residues are attacked with a significantly reduced affinity. The resulting 2-O-acetylated xylan was used to investigate for the first time the migration of the 2-O-acetyl group to position 3 within the polysaccharide. In contrast to easy acetyl group migration along the monomeric xylopyranosides or non-reducing-end terminal Xylp residues of xylooligosaccharides, such a migration in the polymer required much longer heating at 100 °C. The specificity of the xylan 3-O-deacetylase was, however, no so strict on acetylated methyl and 4-nitrophenyl xylopyranosides.

Partial acetylation of β-L(and D)-arabinose and methyl β-L(and D)-arabinopyranoside, and related 13C-n.m.r. studies

Lee, Elizabeth E.,Wood, John O.

, p. 329 - 333 (2007/10/02)

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