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Thiocyanic acid 4-chloro-2-nitrophenyl ester is a chemical compound with the molecular formula C7H4ClN2O2S. It is an ester derivative of thiocyanic acid, featuring a 4-chloro-2-nitrophenyl group attached to the thiocyanate ion. Thiocyanic acid 4-chloro-2-nitrophenyl ester is characterized by its yellow crystalline appearance and is soluble in organic solvents such as ethanol and acetone. It is primarily used in the synthesis of various organic compounds and as an intermediate in chemical reactions. Due to its potential reactivity and the presence of functional groups like nitro and chloro, it is important to handle Thiocyanic acid 4-chloro-2-nitrophenyl ester with care, following proper safety protocols.

6803-43-6

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6803-43-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6803-43-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,0 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6803-43:
(6*6)+(5*8)+(4*0)+(3*3)+(2*4)+(1*3)=96
96 % 10 = 6
So 6803-43-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H3ClN2O2S/c8-5-1-2-7(13-4-9)6(3-5)10(11)12/h1-3H

6803-43-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-chloro-2-nitrophenyl) thiocyanate

1.2 Other means of identification

Product number -
Other names Thiocyanic acid,4-chloro-2-nitrophenyl ester

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:6803-43-6 SDS

6803-43-6Relevant academic research and scientific papers

Design, synthesis, and SAR of cis-1,2-diaminocyclohexane derivatives as potent factor Xa inhibitors. Part I: Exploration of 5-6 fused rings as alternative S1 moieties

Yoshikawa, Kenji,Yokomizo, Aki,Naito, Hiroyuki,Haginoya, Noriyasu,Kobayashi, Shozo,Yoshino, Toshiharu,Nagata, Tsutomu,Mochizuki, Akiyoshi,Osanai, Ken,Watanabe, Kengo,Kanno, Hideyuki,Ohta, Toshiharu

experimental part, p. 8206 - 8220 (2010/04/06)

A series of cis-1,2-diaminocyclohexane derivatives were synthesized with the aim of optimizing previously disclosed factor Xa (fXa) inhibitors. The exploration of 5-6 fused rings as alternative S1 moieties resulted in two compounds which demonstrated improved solubility and reduced food effect compared to the clinical candidate, compound A. Herein, we describe the synthesis and structure-activity relationship (SAR), together with the physicochemical properties and pharmacokinetic (PK) profiles of some prospective compounds.

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