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610-14-0

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610-14-0 Usage

General Description

Crystalline solid. 2-Nitrobenzoyl chloride is shock sensitive.

Air & Water Reactions

Insoluble in water. Decomposes in water.

Reactivity Profile

2-Nitrobenzoyl chloride is incompatible with bases (including amines), with strong oxidizing agents, and with alcohols. May react with reducing agents. May react vigorously or explosively if mixed with diisopropyl ether or other ethers in the presence of trace amounts of metal salts [J. Haz. Mat., 1981, 4, 291].

Health Hazard

ACUTE/CHRONIC HAZARDS: 2-Nitrobenzoyl chloride is an irritant to skin, eyes and tissues.

Fire Hazard

Flash point data is not available for 2-Nitrobenzoyl chloride, but 2-Nitrobenzoyl chloride is probably combustible.

Check Digit Verification of cas no

The CAS Registry Mumber 610-14-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 610-14:
(5*6)+(4*1)+(3*0)+(2*1)+(1*4)=40
40 % 10 = 0
So 610-14-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H4ClNO3/c8-7(10)5-3-1-2-4-6(5)9(11)12/h1-4H

610-14-0 Well-known Company Product Price

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  • Sigma-Aldrich

  • (73100)  2-Nitrobenzoylchloride  purum, ≥97.0% (T)

  • 610-14-0

  • 73100-250ML

  • 8,207.55CNY

  • Detail
  • Aldrich

  • (322717)  2-Nitrobenzoylchloride  97%

  • 610-14-0

  • 322717-5G

  • 435.24CNY

  • Detail
  • Aldrich

  • (322717)  2-Nitrobenzoylchloride  97%

  • 610-14-0

  • 322717-25G

  • 1,422.72CNY

  • Detail

610-14-0SDS

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-Nitrobenzoyl chloride

1.2 Other means of identification

Product number -
Other names 2-Nitrobenzoylchloride

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:610-14-0 SDS

610-14-0Relevant articles and documents

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Ross

, p. 5998,6000 (1970)

-

Divergent Syntheses of Indoles and Quinolines Involving N1-C2-C3 Bond Formation through Two Distinct Pd Catalyses

San Jang, Su,Kim, Young Ho,Youn, So Won

, p. 9151 - 9157 (2020/11/03)

Pd-catalyzed annulative couplings of 2-alkenylanilines with aldehydes using alcohols as both the solvent and hydrogen source have been developed. These domino processes allow divergent syntheses of two significant N-heterocycles, indoles and quinolines, from the same substrate by tuning reaction parameters, which seems to invoke two distinct mechanisms. The nature of the ligand and alcoholic solvent had a profound influence on the selectivity and efficiency of these protocols. Particularly noteworthy is that indole formation was achieved by overcoming two significant challenges, regioselective hydropalladation of alkenes and subsequent reactions between the resulting Csp3-Pd species and less reactive imines.

BENZOCARBONYL COMPOUNDS

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Paragraph 00497, (2019/06/23)

Provided herein are compounds and pharmaceutical compositions comprising said compounds that are useful for treating cancers. Specific cancers include those that are mediated by YAP/TAZ or those that are modulated by the interaction between YAP/TAZ and TEAD.

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