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1-Pyrrolidineacetonitrile,3-hydroxy-,(3S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

540787-77-7

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540787-77-7 Usage

Synonym

(S)-3-Hydroxy Pyrrolidine-1-Acetonitrile

Derivative of

Pyrrolidine

Chiral compound

Yes

Stereochemistry

3S

Class of organic compounds

Alpha amino nitriles

Industrial uses

Pharmaceutical and chemical industries

Possible applications

Intermediate in the synthesis of pharmaceutical compounds and organic molecules, building block in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 540787-77-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,0,7,8 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 540787-77:
(8*5)+(7*4)+(6*0)+(5*7)+(4*8)+(3*7)+(2*7)+(1*7)=177
177 % 10 = 7
So 540787-77-7 is a valid CAS Registry Number.

540787-77-7Upstream product

540787-77-7Relevant academic research and scientific papers

ANTHARQUINONE COMPOUNDS AS ANTI CANCER COMPOUNDS

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Page/Page column 11; 14-15, (2008/06/13)

Anthraquinone compounds of the general formula (I) or a salt thereof (Formula I) in which R1 to R4 are each selected from the group consisting of H, C1-4 alkyl, X1, -NHR0N (R5)2 in which R0 is a C1-12 alkanediyl and each R5 is H or optionally substituted C1-4 alkyl, and a group of formula (II) in which at least one of R6,R7 and R8 is selected from X2 , and X2 substituted C1-4 alkyl and any others are H or C1-4 alkyl; R9 is selected from H, C1-4 alkyl, X2 and X2 substituted C1-4 alkyl; m is 0 or 1; n is 1 or 2; X1 is a halogen atom, a hydroxyl group, a C1-6 alkoxyl group, an aryloxy group or an acyloxy group; and X2 is a halogen atom, a hydroxyl group, a C1-6 alkoxyl group, an aryloxy group or an acyloxy group; provided that at least one of R1 to R4 is a group of formula (II). The N-oxides are useful prodrugs which are selectively bioreduced in hypoxic tumours to the corresponding cyclic amine derivatives. The amine compounds are cytotoxic and may be used as alkylating agents having topoisomerase II inhibiting activities in cancer therapy.

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