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1H-Pyrrole-2,5-dicarboxylic acid, 3-(2-methoxy-2-oxoethyl)-4-(3-methoxy-3-oxopropyl)-, 2-(phenylmethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62618-55-7

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62618-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62618-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,1 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62618-55:
(7*6)+(6*2)+(5*6)+(4*1)+(3*8)+(2*5)+(1*5)=127
127 % 10 = 7
So 62618-55-7 is a valid CAS Registry Number.

62618-55-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-benzyloxycarbonyl-4-methoxycarbonylmethyl-3-(2-methoxycarbonylethyl)pyrrole-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-(2-Methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-1H-pyrrole-2,5-dicarboxylic acid 5-benzyl ester

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:62618-55-7 SDS

62618-55-7Relevant academic research and scientific papers

Synthetic and Biosynthetic Studies of Porphyrins. Part 8. Synthese of Hepta-, Hexa-, and penta-carboxylic Porphyrins Related to Urophorphin-I

Jackson, Anthony H.,Supphayen, Damrus

, p. 277 - 286 (1987)

The title porphyrins of interest as abnormal metabolits in porphyrins biosynthesis, have been synthesized by the Fischer, and b-oxobilane routes, and compared with the naturally derived materials.Enzymic experiments have shown that the conversion of uropo

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