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4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2S)-carboxy-3-thienylacetyl]amino]-6-methoxy-3,3-dimethyl-7-oxo-, (2S,5R,6S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94536-98-8

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94536-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94536-98-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,5,3 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 94536-98:
(7*9)+(6*4)+(5*5)+(4*3)+(3*6)+(2*9)+(1*8)=168
168 % 10 = 8
So 94536-98-8 is a valid CAS Registry Number.

94536-98-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name rac-6β-((Ξ)-2-carboxy-2-thiophen-3-yl-acetylamino)-6α-methoxy-penicillanic acid

1.2 Other means of identification

Product number -
Other names (2S,5R,6S)-6-(2-Carboxy-2-thiophen-3-yl-acetylamino)-6-methoxy-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid

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:94536-98-8 SDS

94536-98-8Downstream Products

94536-98-8Relevant academic research and scientific papers

Process for the preparatin of β-lactam compounds

-

, (2008/06/13)

The present invention provides a process for the substitution of an acylamino β-lactam compound at the carbon atom carrying the acylamino group, which process comprises reacting the β-lactam compound with an halogenating agent and a nucleophilic reagent; characterized in that the acylamino group has an acidic group on the carbon atom adjacent the carbonyl group. In particular the process of this invention comprises reacting a β-lactam of partial structure (I): STR1 where X represents an acidic group; with an halogenating agent and a nucleophilic reagent.

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