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1501-41-3

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1501-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1501-41-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,0 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1501-41:
(6*1)+(5*5)+(4*0)+(3*1)+(2*4)+(1*1)=43
43 % 10 = 3
So 1501-41-3 is a valid CAS Registry Number.

1501-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(bromomethyl)-1-methylquinoxalin-2(1H)-one

1.2 Other means of identification

Product number -
Other names 3-bromomethyl-1-methyl-1H-quinoxalin-2-one

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:1501-41-3 SDS

1501-41-3Relevant articles and documents

C?H Methylation of Iminoamido Heterocycles with Sulfur Ylides**

Ghosh, Prithwish,Kwon, Na Yeon,Kim, Saegun,Han, Sangil,Lee, Suk Hun,An, Won,Mishra, Neeraj Kumar,Han, Soo Bong,Kim, In Su

supporting information, p. 191 - 196 (2020/10/29)

The direct methylation of N-heterocycles is an important transformation for the advancement of pharmaceuticals, agrochemicals, functional materials, and other chemical entities. Herein, the unprecedented C(sp2)-H methylation of iminoamido heterocycles as nucleoside base analogues is described. Notably, trimethylsulfoxonium salt was employed as a methylating agent under aqueous conditions. A wide substrate scope and excellent level of functional-group tolerance were attained. Moreover, this method can be readily applied to the site-selective methylation of azauracil nucleosides. The feasibility of gram-scale reactions and various transformations of the products highlight the synthetic potential of the developed method. Combined deuterium-labeling experiments aided the elucidation of a plausible reaction mechanism.

Novel compounds for enhancing chemotherapy

-

, (2008/06/13)

The present invention provides chemical compounds, pharmaceutical compositions, and methods for increasing the therapeutic efficacy of drugs. Specifically, the invention provides compounds and compositions for inhibiting drug transport proteins that efflu

Quinoxalinone compounds useful for expanding the lumina or air passages in mammals

-

, (2008/06/13)

Compounds of the formula below are useful for expanding the lumina or air passages in a mammal in need of said treatment. The compounds are also useful for treating atopic eczema and urticaria. STR1 wherein X and Y are the same or different and are hydrogen, fluoro, chloro, bromo, nitro, trifluoromethyl, alkyl of one to four carbon atoms, inclusive, alkoxy of one to four carbon atoms, inclusive, and cyano; R1 is hydrogen, methyl or ethyl; R2 is hydrogen, alkyl of one to six carbon atoms, inclusive, phenyl, benzyl, CH2 Z wherein Z is fluoro, chloro, or bromo, CO2 M, CH2 CO2 M, CH2 CH2 CO2 M and CHR3 CO2 M wherein M is hydrogen, alkyl of one to four carbon atoms, inclusive, or a physiologically acceptable metal or amine cation and R3 is alkyl of one to three carbon atoms, inclusive, with the proviso that M is not hydrogen when R2 is CH2 CO2 M or a CHR3 CO2 M.

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