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107324-93-6

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107324-93-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107324-93-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,3,2 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 107324-93:
(8*1)+(7*0)+(6*7)+(5*3)+(4*2)+(3*4)+(2*9)+(1*3)=106
106 % 10 = 6
So 107324-93-6 is a valid CAS Registry Number.

107324-93-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-nitrophenyl)propionic acid chloride

1.2 Other means of identification

Product number -
Other names .3-(p-nitrophenyl)propanoyl chloride

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:107324-93-6 SDS

107324-93-6Relevant articles and documents

FGFR INHIBITOR AND APPLICATION THEREOF

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Paragraph 0276; 0278, (2020/01/22)

An azatricyclic compound (as represented by formula I) which acts as an inhibitor of fibroblast growth factor receptors (FGFR), as well as a pharmaceutical composition thereof, a preparation method, and a use therefor in the treatment of FGFR-mediated diseases. The azatricyclic compound exerts an effect by means of participating in the regulation of a plurality of processes such as cell proliferation, apoptosis, migration, neovascularization, and the like. AA%%%Formula (I).

PROCESSES FOR PREPARING PEPTIDE CONJUGATES AND LINKERS

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Paragraph 0173-0177, (2015/02/19)

The present invention provides a process for preparing a compound of Formula 5b, as well as intermediates thereof, and novel classes of compounds useful in process for preparing these and similar compounds.

Chromatography- and lyophilization-free synthesis of a peptide- linker conjugate

Magano, Javier,Bock, Brandon,Brennan, John,Farrand, Douglas,Lovdahl, Michael,Maloney, Mark T.,Nadkarni, Durgesh,Oliver, Wendy K.,Pozzo, Mark J.,Teixeira, John J.,Wang, Jian,Rizzo, John,Tumelty, David

, p. 142 - 151 (2014/05/20)

An optimized and scalable process to manufacture peptide-linker conjugate 1 is reported that avoids the chromatographic purification and lyophilization that are typically required for the isolation of this type of compound. An operationally simple protoco

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