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56443-24-4

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56443-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56443-24-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,4 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56443-24:
(7*5)+(6*6)+(5*4)+(4*4)+(3*3)+(2*2)+(1*4)=124
124 % 10 = 4
So 56443-24-4 is a valid CAS Registry Number.

56443-24-4SDS

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 2-bromo-1-(2-phenylmethoxyphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 2'-benzyloxy-2-bromoacetophenone

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:56443-24-4 SDS

56443-24-4Relevant articles and documents

COMPOSITIONS AND METHODS FOR TREATING CANCER

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Page/Page column 00803; 00804, (2019/03/12)

Provided herein are compositions and methods for treating, inhibiting and/or reducing the severity of neuroblastoma, small cell lung cancer (SCLC), large cell neuroendocrine cancer (LCNEC), large-cell carcinoma (LCC), squamous cell carcinoma (SqCC), and/o

COMPOSITIONS AND METHODS OF REGULATING CANCER RELATED DISORDERS AND DISEASES

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Paragraph 136, (2017/08/01)

Provided herein are naphthylic derivative compounds, or pharmaceutically acceptable salts thereof, that are useful for inhibiting cancers. Also provided herein are methods of using effective amounts of said compounds, optionally with pharmaceutical carrie

A xanthate-based free radical approach to defucogilvocarcin M

Cortezano-Arellano, Omar,Cordero-Vargas, Alejandro

supporting information; experimental part, p. 602 - 604 (2010/04/05)

A formal total synthesis of the aglycon of gilvocarcin M is described. The synthesis is based on the construction of the key naphthalene 7 via a free radical addition-cyclization protocol followed by aromatization of the resulting α-tetralone. This highly

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