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6361-21-3

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6361-21-3 Usage

Chemical Properties

light yellow to beige-yellow crystalline powder

Uses

2-Chloro-5-nitrobenzaldehyde was used in the synthesis of 5-nitro-2-(1H-pyrrol-1-yl)benzaldehyde.

General Description

2-Chloro-5-nitrobenzaldehyde undergoes condensation reaction with 2-methyl-1-propenylbenzimidazole to yield (E,Z)-2-(2-chloro-5-nitrostyryl)-1-(1-propenyl)benzimidazole. It reacts with 5-aminopyrazoles to yield symmetrical bispyrazolo[3,4-]pyridines.

Check Digit Verification of cas no

The CAS Registry Mumber 6361-21-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,6 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6361-21:
(6*6)+(5*3)+(4*6)+(3*1)+(2*2)+(1*1)=83
83 % 10 = 3
So 6361-21-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H4ClNO3/c8-7-2-1-6(9(11)12)3-5(7)4-10/h1-4H

6361-21-3 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (A14824)  2-Chloro-5-nitrobenzaldehyde, 97%   

  • 6361-21-3

  • 10g

  • 258.0CNY

  • Detail
  • Alfa Aesar

  • (A14824)  2-Chloro-5-nitrobenzaldehyde, 97%   

  • 6361-21-3

  • 50g

  • 946.0CNY

  • Detail
  • Alfa Aesar

  • (A14824)  2-Chloro-5-nitrobenzaldehyde, 97%   

  • 6361-21-3

  • 100g

  • 1349.0CNY

  • Detail

6361-21-3SDS

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 2-Chloro-5-nitrobenzaldehyde

1.2 Other means of identification

Product number -
Other names 2-chloro-5-nitrobenzaldehyde

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:6361-21-3 SDS

6361-21-3Relevant articles and documents

NEW FYN AND VEGFR2 KINASE INHIBITORS

-

Page/Page column 25; 26, (2021/06/22)

The invention relates to a N-phenylcarbamoyl compound of Formula (I) or a pharmaceutically acceptable salt thereof for use in the inhibition of at least one of tyrosine kinase selected from Fyn and VEGFR2 in the treatment of diseases and disorders involved with one or both kinases. (Formula)

Efficient and Highly Selective Solvent-Free Oxidation of Primary Alcohols to Aldehydes Using Bucky Nanodiamond

Lin, Yangming,Wu, Kuang-Hsu Tim,Yu, Linhui,Heumann, Saskia,Su, Dang Sheng

, p. 3497 - 3505 (2017/09/15)

Selective oxidation of alcohols to aldehydes is widely applicable to the synthesis of various green chemicals. The poor chemoselectivity for complicated primary aldehydes over state-of-the-art metal-free or metal-based catalysts represents a major obstacle for industrial application. Bucky nanodiamond is a potential green catalyst that exhibits excellent chemoselectivity and cycling stability for the selective oxidation of primary alcohols in diverse structures (22 examples, including aromatic, substituted aromatic, unsaturated, heterocyclic, and linear chain alcohols) to their corresponding aldehydes. The results are comparable to reported transition-metal catalysts including conventional Pt/C and Ru/C catalysts for certain substrates under solvent-free conditions. The possible activation process of the oxidant and substrates by the surface oxygen groups and defect species are revealed with model catalysts, ex situ electrochemical measurements, and ex situ attenuated total reflectance. The zigzag edges of sp2 carbon planes are shown to play a key role in these reactions.

Isoquinoline compound melanocortin receptor ligands and methods of using same

-

, (2008/06/13)

The invention relates to melanocortin receptor ligands and methods of using the ligands to alter or regulate the activity of a melanocortin receptor. The invention further relates to tetrahydroisoquinoline aromatic amines that function as melanocortin receptor ligands and as agents for controlling cytokine-regulated physiologic processes and pathologies, and combinatorial libraries thereof.

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