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10-Methyl-11-deazahomofolic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119770-55-7

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119770-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119770-55-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,7,7 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 119770-55:
(8*1)+(7*1)+(6*9)+(5*7)+(4*7)+(3*0)+(2*5)+(1*5)=147
147 % 10 = 7
So 119770-55-7 is a valid CAS Registry Number.
InChI:InChI=1/C22H24N6O6/c1-11(9-14-10-24-18-17(25-14)20(32)28-22(23)27-18)8-12-2-4-13(5-3-12)19(31)26-15(21(33)34)6-7-16(29)30/h2-5,10-11,15H,6-9H2,1H3,(H,26,31)(H,29,30)(H,33,34)(H3,23,24,27,28,32)/t11?,15-/m0/s1

119770-55-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[[4-[3-(2-amino-4-oxo-1H-pteridin-6-yl)-2-methylpropyl]benzoyl]amino]pentanedioic acid

1.2 Other means of identification

Product number -
Other names 10-Methyl-11-deazahomofolic 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:119770-55-7 SDS

119770-55-7Relevant academic research and scientific papers

Folate analogues. 31. Synthesis of the reduced derivatives of 11-deazahomofolic acid, 10-methyl-11-deazahomofolic acid, and their evaluation as inhibitors of glycinamide ribonucleotide formyltransferase

Nair,Murthy,Patil,Kisliuk,Thorndike,Gaumont,Ferone,Dutch,Edelstein

, p. 1277 - 1283 (2007/10/02)

The Boon-Leigh procedure, involving condensation of a 6-chloro-5-nitropyrimidine (22) with an α-amino ketone (20 or 21) followed by reduction of the nitro group, cyclization, and L-glutamylation, led to the formation of 11-deazahomofolate (29) and its 10-

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