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79384-36-4

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79384-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79384-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,8 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79384-36:
(7*7)+(6*9)+(5*3)+(4*8)+(3*4)+(2*3)+(1*6)=174
174 % 10 = 4
So 79384-36-4 is a valid CAS Registry Number.

79384-36-4SDS

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 O-3-acetamido-2,4,6-tri-O-benzyl-3-deoxy-α-D-glucopyranosyl-(1->6)-1,3,2',6'-tetrakis-N-benzyloxycarbonylgentamine C1a

1.2 Other means of identification

Product number -
Other names -

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:79384-36-4 SDS

79384-36-4Downstream Products

79384-36-4Relevant articles and documents

Semisynthetic Aminoglycoside Antibacterials. Part 7. Synthesis of Novel Hexopyranosyl and Hexofuranosyl Derivatives of Gentamine C1 and C1a

Daniels, Peter J. L.,Luce, Charles E.,Mallams, Alan K.,Morton, James B.,Saluja, Surinderjit S.,at al.

, p. 2137 - 2150 (2007/10/02)

Acidic hydrolysis of gentamicin C1 and C1a provides ready access to the pseudodisaccharides gentamine C1 and C1a respectively.Glycosylation of tetrakis-N-benzyloxycarbonylgentamine C1 and C1a using the Koenigs-Knorr or Lemieux-Nagabhushan reactions has led to the preparation of a series of novel 6-O-α- and -β-3-amino-3-deoxy- and 2-amino-2-deoxy-D-hexopyranosyl and hexofuranosyl analogues of the gentamicins.The 13C n.m.r. properties of representative compounds are described and the rotamer populations about the C-4-O and C-6-O glycosidic bonds are discussed.

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