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1000980-60-8

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1000980-60-8 Usage

Uses

Different sources of media describe the Uses of 1000980-60-8 differently. You can refer to the following data:
1. A Ceftazidime isomer, an impurity of Ceftazidime (C244100).
2. 2-Ceftazidime, 90% (Ceftazidime EP Impurity A) is a Ceftazidime isomer, an impurity of Ceftazidime (C244100).

Check Digit Verification of cas no

The CAS Registry Mumber 1000980-60-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,9,8 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1000980-60:
(9*1)+(8*0)+(7*0)+(6*0)+(5*9)+(4*8)+(3*0)+(2*6)+(1*0)=98
98 % 10 = 8
So 1000980-60-8 is a valid CAS Registry Number.

1000980-60-8SDS

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 (6R,7R)-7-[2-(2-amino-4-thiazolyl)-2-(Z)-(2,2-dimethylacetoxyimino)acetamido]-3-[(pyridinium)methyl]-2-cephem-4-carboxylate

1.2 Other means of identification

Product number -
Other names CEFTAZIDIME IMPURITY A

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:1000980-60-8 SDS

1000980-60-8Upstream product

1000980-60-8Downstream Products

1000980-60-8Relevant articles and documents

Novel approach for the conversion of natural Δ3 cephalosporin derivatives into corresponding Δ2 cephalosporin derivatives

Prasada Rao, Korrapati V. V.,Dandala, Ramesh,Handa, Vijay K.,Kamat, Anand G.,Subramanyeswara Rao, Inti V.,Rani, Ananta,Naidu, Andra

, p. 1513 - 1515 (2008/09/18)

(Chemical Equation Presented) A simple one pot synthetic method for the isomerization of cephem double bond from the natural 3-position to 2-cephem positions is affected by silylation. Thus cephalosporin acids are treated with N-trimethylsilylacetamide (MSA) or N,O-bis(trimethylsilyl)acetamide (BSA) and the resulting silyl esters are treated with triethylamine at ambient temperature in the same pot to afford Δ2-cephalosporins, which are potentially related compounds in cephalosporin antibacterial compounds.

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