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2-Chloro-5-nitrobenzoyl chloride

2-Chloro-5-nitrobenzoyl chloride Suppliers list
Company Name: Jiangsu 01 Industrial Co., Ltd  Gold
Tel: 0523-87653988 15105181882
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Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Tel: 4006356688 18621169109
Email: market03@meryer.com
Company Name: Bridge Organics  
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Email: ab@bridgeorganics.com
Company Name: Alfa Aesar  
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Email: saleschina@alfa-asia.com

2-Chloro-5-nitrobenzoyl chloride manufacturers

2-Chloro-5-nitrobenzoyl chloride Basic information
Product Name:2-Chloro-5-nitrobenzoyl chloride
Synonyms:2-CHLORO-5-NITROBENZOYL CHLORIDE;2-chloro-5-nitro-benzoylchlorid;Benzoyl chloride, 2-chloro-5-nitro-;2-Chloro-5-Nitrobenzoyl;2-Chloro-5-nitrobenzoic acid chloride;2-Chloro-5-nitrobenzoyl Chloride >;SKL1284
CAS:25784-91-2
MF:C7H3Cl2NO3
MW:220.01
EINECS:247-262-4
Product Categories:
Mol File:25784-91-2.mol
2-Chloro-5-nitrobenzoyl chloride Structure
2-Chloro-5-nitrobenzoyl chloride Chemical Properties
Melting point 58-60°C
Boiling point 157-158°C 11mm
density 1.575±0.06 g/cm3(Predicted)
Fp 157-158°C/11mm
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form powder to crystal
color White to Orange to Green
Sensitive Moisture Sensitive
BRN 2213721
InChIInChI=1S/C7H3Cl2NO3/c8-6-2-1-4(10(12)13)3-5(6)7(9)11/h1-3H
InChIKeyOGLKKYALUKXVPQ-UHFFFAOYSA-N
SMILESC(Cl)(=O)C1=CC([N+]([O-])=O)=CC=C1Cl
CAS DataBase Reference25784-91-2(CAS DataBase Reference)
NIST Chemistry Reference2-Chloro-5-nitrobenzoyl chloride(25784-91-2)
EPA Substance Registry SystemBenzoyl chloride, 2-chloro-5-nitro- (25784-91-2)
Safety Information
Hazard Codes C,Xi
Risk Statements 34-41
Safety Statements 26-36/37/39-45
RIDADR 3261
TSCA TSCA listed
HS Code 2916.39.7900
HazardClass 8
PackingGroup II
MSDS Information
ProviderLanguage
2-Chloro-5-nitrobenzoyl chloride English
ALFA English
2-Chloro-5-nitrobenzoyl chloride Usage And Synthesis
Biological Activity2-Chloro-5-nitrobenzoyl chloride (2CNBCl) is an amide that contains a terminal alkyne. It is synthesized from the corresponding thionyl chloride and ethanolamine in the presence of carbon tetrachloride. 2CNBCl has been shown to inhibit the growth of various cancer cell lines, including those derived from melanoma, lung, breast, and colon cancer cells. 2CNBCl also inhibits the production of growth factor proteins such as platelet-derived growth factor (PDGF). 2CNBCl has also been shown to inhibit DNA synthesis by interacting with enzymes involved in the process.
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