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75504-01-7

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75504-01-7 Usage

General Description

2-(1-Bromo-ethyl)-pyridine is a chemical compound with the molecular formula C7H8BrN. It is an organic compound that consists of a pyridine ring with a bromoethyl substituent. 2-(1-BroMo-ethyl)-pyridine is commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is flammable and should be stored and handled with care. 2-(1-Bromo-ethyl)-pyridine is also used in research and development processes for its unique chemical properties and reactivity. It is important to handle this chemical with appropriate safety precautions and in accordance with relevant regulations and guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 75504-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,5,0 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75504-01:
(7*7)+(6*5)+(5*5)+(4*0)+(3*4)+(2*0)+(1*1)=117
117 % 10 = 7
So 75504-01-7 is a valid CAS Registry Number.

75504-01-7SDS

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 2-(1-Bromoethyl)pyridine

1.2 Other means of identification

Product number -
Other names 2-(1-bromo-ethyl)-pyridine

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:75504-01-7 SDS

75504-01-7Relevant articles and documents

Development of 2,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one inhibitors of aldehyde dehydrogenase 1A (ALDH1A) as potential adjuncts to ovarian cancer chemotherapy

Buchman, Cameron D.,Buckanovich, Ronald J.,Chtcherbinine, Mikhail,Debnath, Bikash,Felton, Jeremy,Grimley, Edward,Huddle, Brandt C.,Hurley, Thomas D.,Larsen, Scott D.,Li, Siwei,Mao, Shuai,McGonigal, Stacy C.,Neamati, Nouri,Pan, Shu,Sun, Duxin,Takahashi, Cyrus,Wen, Bo

, (2020/12/21)

There is strong evidence that inhibition of one or more Aldehyde Dehydrogenase 1A (ALDH1A) isoforms may be beneficial in chemotherapy-resistant ovarian cancer and other tumor types. While many previous efforts have focused on development of ALDH1A1 select

SMALL MOLECULE INHIBITORS OF ALDH AND USES THEREOF

-

Page/Page column 101, (2018/04/12)

This invention is in the field of medicinal chemistry. In particular, the invention relates to a new class of small-molecules having a thiopyrimidinone structure which function as inhibitors of ALDH protein, and their use as therapeutics for the treatment of cancer and other diseases.

N-alkylation of lactams with secondary heterobenzylic bromides

Yu, Ming,Stevenson, Karis,Zhou, Gene

, p. 5591 - 5594 (2014/12/11)

We herein report a general N-alkylation reaction of lactams with secondary heterobenzylic bromides. This methodology features mild reaction condition, moderate to high product isolation yield, and broad substrate scope. Good chemical and structural tolerance has also been demonstrated by both the secondary heterobenzylic bromides and lactam substrates.

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