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110224-25-4

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110224-25-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110224-25-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,2,2 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 110224-25:
(8*1)+(7*1)+(6*0)+(5*2)+(4*2)+(3*4)+(2*2)+(1*5)=54
54 % 10 = 4
So 110224-25-4 is a valid CAS Registry Number.

110224-25-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chlorovaleric acid p-toluidide

1.2 Other means of identification

Product number -
Other names 5-chloro-valeric acid p-toluidide

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:110224-25-4 SDS

110224-25-4Relevant articles and documents

Efficient nitriding reagent and application thereof

-

Paragraph 0445-0448, (2021/03/31)

The invention discloses an efficient nitriding reagent and application thereof, wherein the nitriding reagent comprises nitrogen oxide, an active agent, a reducing agent and an organic solvent. By applying the nitriding reagent, nitrogen-containing compounds such as amide, nitrile and the like can be produced, and the method is simple in condition, low in waste discharge amount and simple in reaction equipment.

A one pot protocol to convert nitro-arenes into: N-aryl amides

Massolo, Elisabetta,Pirola, Margherita,Puglisi, Alessandra,Rossi, Sergio,Benaglia, Maurizio

, p. 4040 - 4044 (2020/02/04)

A two-step one pot, experimentally simple protocol, based on readily available and inexpensive reagents allowed the conversion of nitro-arenes directly to N-aryl amides. A metal-free reduction of the nitro group, mediated by trichlorosilane, followed by the addition of an anhydride afforded the corresponding N-aryl carboxyamide, that was isolated after a simple aqueous work up in good-excellent yields. When the methodology was applied to the reaction with γ-butyrolactone, the desired N-aryl butanamide derivative was obtained, featuring a chlorine atom at the γ-position, a functionalized handle that can be used for further synthetic manipulation of the reaction product. Such an intermediate has already been employed as a key advanced precursor of pharmaceutically active compounds.

Congener derivatives and conjugates of histamine: Synthesis and tissue and receptor selectivity of the derivatives

Khan,Melmon,Marr-Leisy,Verlander,Egli,Lok,Goodman

, p. 2115 - 2120 (2007/10/02)

A series of 19 congener derivatives and conjugates of histamine was synthesized and tested to determine whether the ligands would alter the conventional histamine activity in various tissues. The derivatives, which contained either branched or unbranched

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