Welcome to LookChem.com Sign In|Join Free

CAS

  • or

103772-10-7

Post Buying Request

103772-10-7 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

103772-10-7 Usage

General Description

5-Nitro-2,3,4,5-tetrafluoro benzoyl chloride is a chemical compound with the molecular formula C7H3ClF4NO3. It is a yellow to light brown colored liquid with a pungent odor and is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 5-NITRO-2,3,4,5-TETRAFLUORO BENZOYL CHLORIDE is a highly reactive and corrosive compound that is incompatible with water, strong oxidizing agents, and strong bases. It is primarily used in the production of various pharmaceutical drugs and in the manufacturing of certain organic compounds. Its use should be handled with caution and appropriate safety measures due to its highly reactive nature and potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 103772-10-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,7,7 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 103772-10:
(8*1)+(7*0)+(6*3)+(5*7)+(4*7)+(3*2)+(2*1)+(1*0)=97
97 % 10 = 7
So 103772-10-7 is a valid CAS Registry Number.
InChI:InChI=1/C7ClF4NO3/c8-7(14)1-2(9)3(10)4(11)5(12)6(1)13(15)16

103772-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,5,6-tetrafluoro-3-nitrocyclohexa-1,5-diene-1-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 2-nitro-3,4,5,6-tetrafluorobenzoyl chloride

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:103772-10-7 SDS

103772-10-7Relevant articles and documents

Synthesis and biological activity of 5-amino- and 5-hydroxyquinolones, and the overwhelming influence of the remote N1-substituent in determining the structure-activity relationship

Domagala,Bridges,Culbertson,Gambino,Hagen,Karrick,Porter,Sanchez,Sesnie,Spense,Szotek,Wemple

, p. 1142 - 1154 (2007/10/02)

A series of 5-amino- and 5-hydroxyquinolone antibacterials substituted at C7 with a select group of common piperazinyl and 3-aminopyrrolidinyl side chains was prepared. These 5-substituted derivatives were compared to the analogous 5-hydrogen compounds for antiinfective activity by using DNA gyrase inhibition, minimum inhibitory concentrations against a variety of bacteria, and in vivo efficacy in the mouse infection model. The influence on the structure-activity relationships of varied substituents at C8 (H, F, Cl) and N1 (ethyl, cyclopropyl, difluorophenyl) was also studied. The results showed that several of the structure-activity conclusions regarding side-chain bulk at C7, the effect of halogen at C8, and the effect of the C5-amino group were greatly influenced by the choice of the N1-substituent. Several outstanding broad spectrum quinolones were identified in this work. In particular, the spectrum and potency of the 7-piperazinyl quinolones could be greatly enhanced by the judicious choice of C5-, C8-, and N1-substitutents.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 103772-10-7