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4-(4-broMophenyl)-2,2-diMethyl-4-oxo-butyric acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

791593-72-1

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791593-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 791593-72-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,1,5,9 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 791593-72:
(8*7)+(7*9)+(6*1)+(5*5)+(4*9)+(3*3)+(2*7)+(1*2)=211
211 % 10 = 1
So 791593-72-1 is a valid CAS Registry Number.

791593-72-1SDS

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 4-(4-bromophenyl)-2,2-dimethyl-4-oxo-butyric acid

1.2 Other means of identification

Product number -
Other names 4-(4-bromophenyl)-2,2-dimethyl-4-oxobutanoic acid

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:791593-72-1 SDS

791593-72-1Downstream Products

791593-72-1Relevant academic research and scientific papers

ANTIBODY DRUG CONJUGATES (ADCS) WITH NAMPT INHIBITORS

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Page/Page column 325-326, (2021/01/29)

Conjugate of a binder having formula (AA) wherein AB stands for a binder, Z' stands for a linker, D stands for an active component which is a NAMPT inhibitor and its use as pharmaceuticals.

DIHYDROPYRIDAZINONES SUBSTITUTED WITH PHENYLUREAS

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Page/Page column 223; 224, (2018/05/27)

Compounds of formula (I) which are nicotinamide phosphoribosyltransferase (NAMPT) inhibitors and their use for the treatment of hyperproloferative diseases and/or disorders responsive to induction of cell death.

Iridium-Catalyzed Asymmetric Hydrogenation of β,γ-Unsaturated γ-Lactams: Scope and Mechanistic Studies

Yuan, Qianjia,Liu, Delong,Zhang, Wanbin

supporting information, p. 1144 - 1147 (2017/03/14)

An efficient asymmetric hydrogenation of β,γ-unsaturated γ-lactams using an iridium-phosphoramidite complex is reported. The chiral γ-lactams were obtained in excellent yields and enantioselectivities (up to 99% yield and 99% ee). The mechanistic studies

Novel inhibitors of 17β-hydroxysteroid dehydrogenase type 1: Templates for design

Allan, Gillian M.,Vicker, Nigel,Lawrence, Harshani R.,Tutill, Helena J.,Day, Joanna M.,Huchet, Marion,Ferrandis, Eric,Reed, Michael J.,Purohit, Atul,Potter, Barry V.L.

, p. 4438 - 4456 (2008/09/21)

The 17β-hydroxysteroid dehydrogenases (17β-HSDs) catalyze the interconversion between the oxidized and reduced forms of androgens and estrogens at the 17 position. The 17β-HSD type 1 enzyme (17β-HSD1) catalyzes the reduction of estrone (E1) to estradiol a

Preparation and use of aryl alkyl acid derivatives for the treatment of obesity

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Page 12, (2008/06/13)

This invention relates to certain aryl alkyl acid compounds, compositions, and methods for treating or preventing obesity and related diseases.

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