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110231-01-1

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110231-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110231-01-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,2,3 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 110231-01:
(8*1)+(7*1)+(6*0)+(5*2)+(4*3)+(3*1)+(2*0)+(1*1)=41
41 % 10 = 1
So 110231-01-1 is a valid CAS Registry Number.

110231-01-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3-morpholin-4-ylpropyl)-2-(3-nitropyrrolo[2,3-b]pyridin-1-yl)acetamide

1.2 Other means of identification

Product number -
Other names 1H-Pyrrolo(2,3-b)pyridine-1-acetamide,N-(3-(4-morpholinyl)propyl)-3-nitro

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:110231-01-1 SDS

110231-01-1Downstream Products

110231-01-1Relevant articles and documents

Nitro derivatives of bi- and tri-cyclic heterocycles as potential radiosensitizers

Yizun, Jin,Adams, Gerald E.,Parrick, John,Stratford, Ian J.

, p. 511 - 516 (2007/10/02)

Two series of bicyclic compounds having a pyridinic and pyrrolic nitrogen atom in different rings have been synthesized as potential radiosensitizers of hypoxic mammalian cells.The compounds were obtained from 3-nitropyrrolopyridine by regioselective alkylation at the nitrogen atom in either the 5- or 6-membered rings.Partition coefficients, one electron reduction potentials, radiosensitization of Chinese hamster V79 cells and cytotoxicity were measured.Generally, the N-1 alkyl-substituted 3-nitropyrrolopyridines showed greater electron affinity than their N-7 alkyl-substituted analogues.All compounds were substantially less electron affinic than the 2-nitroimidazole, misonidazole.Consistent with this, misonidazole showed the most efficient sensitizing properties.None of the compounds synthesized here showed significantly lower toxicity than misonidazole.Consequently there is likely to be no therapeutic benefit from using these novel compounds as radiosensitizers. - 1-alkyl-3-nitro-1H-pyrrolopyridine preparation and radiosensitizer activity/7-alkyl-3-nitro-7H-pyrrolopyridine, preparation and redox properties/3-nitro-1H-pyrrolopyrazine/radiosensitization/cytotoxicity

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