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193624-86-1

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193624-86-1 Usage

General Description

4-Chloro-furo[2,3-b]pyridine is a chemical compound with the molecular formula C7H4ClNO. It is a heterocyclic compound that contains a furo[2,3-b]pyridine ring with a chlorine atom attached to it. 4-CHLORO-FURO[2,3-B]PYRIDINE is often used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used in the development of chemical materials and organic synthesis. 4-Chloro-furo[2,3-b]pyridine has the potential to exhibit various biological activities and is of interest to researchers in the fields of medicinal chemistry and pharmacology.

Check Digit Verification of cas no

The CAS Registry Mumber 193624-86-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,6,2 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 193624-86:
(8*1)+(7*9)+(6*3)+(5*6)+(4*2)+(3*4)+(2*8)+(1*6)=161
161 % 10 = 1
So 193624-86-1 is a valid CAS Registry Number.

193624-86-1SDS

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 4-Chlorofuro[2,3-b]pyridine

1.2 Other means of identification

Product number -
Other names -

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:193624-86-1 SDS

193624-86-1Downstream Products

193624-86-1Relevant articles and documents

Furopyridines. XXIII [1]. Synthesis and Reactions of Chloropyridine Derivatives of Furo[2,3-b]-, -[2,3-c]- and -[3,2-c]pyridine

Shiotani, Shunsaku,Taniguchi, Katsunori

, p. 925 - 929 (1997)

Chlorination of the N-oxides of furo[2,3-b]- 1a, -[2,3-c]- 1b and -[3,2-c]pyridine 1c with phosphorus oxychloride afforded compounds substituted normally at the α- or γ-position to the ring nitrogen, 2a, 2′a, 2b, 2c, 2′c and 2″c, and in addition, in the case of 1b, compounds substituted on the furan ring, 2′b and 2″b. The structures of these compounds were confirmed from their ir, nmr and mass spectra. The major chlorinated products 2a, 2b and 2c were converted to methoxy- 5a, 5b and 5c, N-pyrrolidyl- 7a, 7b and 7c, and phenylthiofuropyridines 8a, 8b, and 8c.

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