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72988-03-5

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  • L-Glutamicacid,N-[4-[[[2-amino-5-[[(2-chloroethyl)amino]carbonyl]-1,4,5,6,7,8-hexahydro-4-oxo-6-pteridinyl]methyl]amino]benzoyl]-(9CI)

    Cas No: 72988-03-5

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  • L-Glutamicacid,N-[4-[[[2-amino-5-[[(2-chloroethyl)amino]carbonyl]-1,4,5,6,7,8-hexahydro-4-oxo-6-pteridinyl]methyl]amino]benzoyl]-(9CI) cas 72988-03-5

    Cas No: 72988-03-5

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72988-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72988-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,9,8 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72988-03:
(7*7)+(6*2)+(5*9)+(4*8)+(3*8)+(2*0)+(1*3)=165
165 % 10 = 5
So 72988-03-5 is a valid CAS Registry Number.

72988-03-5SDS

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 2-[[4-[[2-amino-5-(2-chloroethylcarbamoyl)-4-oxo-1,6,7,8-tetrahydropteridin-6-yl]methylamino]benzoyl]amino]pentanedioic acid

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:72988-03-5 SDS

72988-03-5Downstream Products

72988-03-5Relevant articles and documents

Potential anticancer agents: 5-(N-substituted-aminocarbonyl)- and 5-(N-substituted-aminothiocarbonyl)-5,6,7,8-tetrahydrofolic acids

Temple Jr.,Elliott,Montgomery

, p. 697 - 700 (2007/10/02)

5-[[N-[(Ethoxycarbonyl)alkyl]amino]carbonyl] (6-9) and the corresponding aminothiocarbonyl (12-15) derivatives of 5,6,7,8-tetrahydrofolic acid were prepared as multisubstrate analogues of the substrate-cofactor adduct in the reactions catalyzed by the folate-mediated one-carbon transfer reactions. Evaluation in vitro showed that 7 (alkyl = hexyl) was cytotoxic to H.Ep-2 cells (ED50, 4 μM) but noncytotoxic to proliferating L1210 cells. No activity was observed for 7 against the P388 leukemia in mice.

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