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374777-77-2

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374777-77-2 Usage

General Description

L-Glutamic acid, N-[4-[1-[(2,4-diamino-6-pteridinyl)methyl]-3-butyn-1-yl]benzoyl]-, 1,5-dimethyl ester is a chemical compound that is derived from glutamic acid and pteridines. It is an ester formed by the reaction of 1,5-dimethyl alcohol with the benzoyl group of this compound. This chemical has potential pharmaceutical applications as it contains a pteridine structure, which is a key component in various biological processes. The presence of the benzoyl group also suggests possible medicinal properties due to its known pharmacological effects. Overall, this compound has the potential to be utilized in pharmaceutical research and drug development due to its unique structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 374777-77-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,4,7,7 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 374777-77:
(8*3)+(7*7)+(6*4)+(5*7)+(4*7)+(3*7)+(2*7)+(1*7)=202
202 % 10 = 2
So 374777-77-2 is a valid CAS Registry Number.

374777-77-2SDS

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 10-propargyl-10-deazaaminopterin dimethyl ester

1.2 Other means of identification

Product number -
Other names L-Glutamic acid, N-[4-[1-[(2,4-diamino-6-pteridinyl)methyl]-3-butyn-1-yl]benzoyl]-, 1,5-dimethyl 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:374777-77-2 SDS

374777-77-2Relevant articles and documents

IMPROVED PROCESS FOR THE PREPARATION OF PRALATREXATE

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, (2015/07/15)

An improved process for the preparation of Pralatrexate which is less hazardous. The invention further relates to novel intermediates and process thereof useful for the preparation of Pralatrexate. The present invention also relates to a substantially pure Pralatrexate and a process for obtaining the same in high yield.

PROCESS FOR PREPARATION OF AN ANTIFOLATE AGENT

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, (2014/01/07)

The specification relates to a process for preparation of an antifolate compound of formula 7, such as Pralatrexate. Also, disclosed are intermediates and processes for preparation of intermediates useful in the preparation of the antifolate compound. The substituents Y, Z, R, R1 and R2 are as described herein. The processes and intermediates can provide an alternate route to the synthesis of the antifolate compound. Further, the processes can help to avoid distillation or evaporation of high boiling point solvents, chromatographic purification and use of hazardous combination of solvents; and can also provide a product having high purity, all of which are desirable for synthesis on a large scale.

Treatment of T-cell lymphoma using 10-propargyl-10-deazaaminopterin

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Page/Page column 3; 4; Sheet 2, (2008/06/13)

T cell lymphoma is treated by administering to a patient suffering from T cell lymphoma a therapeutically effective amount of 10-propargyl-10-deazaaminopterin. Remission is observed in human patients, even with drug resistant T cell lymphoma at weekly dosages levels as low as 30 mg/m2. In general, the 10-propargyl-10-deazaaminopterin is administered in an amount of from 30 to 275 mg/m2 per dose.

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