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17815-99-5

17815-99-5

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17815-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17815-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,1 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17815-99:
(7*1)+(6*7)+(5*8)+(4*1)+(3*5)+(2*9)+(1*9)=135
135 % 10 = 5
So 17815-99-5 is a valid CAS Registry Number.

17815-99-5 Well-known Company Product Price

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  • CAS number
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  • Alfa Aesar

  • (H63169)  4-Chloro-N,N-dimethyl-2-nitroaniline, 97%   

  • 17815-99-5

  • 250mg

  • 245.0CNY

  • Detail

  • Alfa Aesar

  • (H63169)  4-Chloro-N,N-dimethyl-2-nitroaniline, 97%   

  • 17815-99-5

  • 1g

  • 735.0CNY

  • Detail

  • Alfa Aesar

  • (H63169)  4-Chloro-N,N-dimethyl-2-nitroaniline, 97%   

  • 17815-99-5

  • 5g

  • 2940.0CNY

  • Detail

17815-99-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-N,N-dimethyl-2-nitroaniline

1.2 Other means of identification

Product number -
Other names 4-chloro-N,N-dimethyl-2-nitrobenzenamine

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:17815-99-5 SDS

17815-99-5Relevant articles and documents

Continuous flow nucleophilic aromatic substitution with dimethylamine generated in situ by decomposition of DMF

Petersen, Trine P.,Larsen, Anders Foller,Ritzen, Andreas,Ulven, Trond

, p. 4190 - 4195 (2013/05/23)

A safe, practical, and scalable continuous flow protocol for the in situ generation of dimethylamine from DMF followed by nucleophilic aromatic substitution of a broad range of aromatic and heteroaromatic halides is reported.

Evidence for radical cations in linked mechanisms of N,N-Dialkyl aromatic amine nitration and nitrosative dealkylation

Loeppky, Richard N.,Singh, Sukhjeet P.,Elomari, Saleh,Hastings, Riley,Theiss, Thomas E.

, p. 5193 - 5202 (2007/10/03)

N,N,-Dialkyl aromatic amines react rapidly with nitrous acid to competitively produced a nitrosamine and a nitro compound. The mechanism of nitro compound formation involves a reaction of an amine radical cation with NO2, while the nitrosamine

α-Mercaptophenylacetic acid derivatives of imidazole-containing compounds and analogues thereof

-

, (2008/06/13)

α-Mercaptobenzylacetic acid derivatives of imidazole-containing compounds and analogues thereof, and their use as immunomodulating agents are disclosed.

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