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67475-56-3

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67475-56-3 Usage

Uses

5-Fluoro-2-methoxybenzenesulfonyl chloride

Check Digit Verification of cas no

The CAS Registry Mumber 67475-56-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,4,7 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67475-56:
(7*6)+(6*7)+(5*4)+(4*7)+(3*5)+(2*5)+(1*6)=163
163 % 10 = 3
So 67475-56-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClFO3S/c1-12-6-3-2-5(9)4-7(6)13(8,10)11/h2-4H,1H3

67475-56-3SDS

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 Benzenesulfonyl chloride, 5-fluoro-2-methoxy-(9CI)

1.2 Other means of identification

Product number -
Other names 5-Fluoro-2-methoxybenzenesulfonyl 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:67475-56-3 SDS

67475-56-3Relevant articles and documents

Metal-Free Twofold Electrochemical C?H Amination of Activated Arenes: Application to Medicinally Relevant Precursor Synthesis

D?rr, Carolin,Diehl, Erika,Hellmich, Ute A.,Schollmeyer, Dieter,Shimizu, Akihiro,Waldvogel, Siegfried R.,Wesenberg, Lars J.,Yoshida, Jun-ichi,Z?hringer, Till J. B.

supporting information, p. 17574 - 17580 (2020/12/07)

The efficient production of many medicinally or synthetically important starting materials suffers from wasteful or toxic precursors for the synthesis. In particular, the aromatic non-protected primary amine function represents a versatile synthetic precu

A novel, flexible strategy to construct privileged dibenzo[b,f][1,4,5]oxathiazepine 5,5-dioxides and their heterocyclic isosteres

Sapegin, Alexander,Panova, Valeria,Reutskaya, Elena,Smirnov, Alexey V.,Krasavin, Mikhail

, p. 7570 - 7578 (2016/11/11)

Secondary o-hydroxybenzene sulfonamides have been explored as bis-electrophilic partners in a practically simple, atom-economical approach to dibenzo[b,f][1,4,5]oxathiazepine-5,5-dioxides and their heterocyclic analogs, which is an underexplored version o

SULFONAMIDE COMPOUNDS AND USES AS TNAP INHIBITORS

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Paragraph 00812, (2013/09/12)

Described herein are compounds that modulate the activity of TNAP. In some embodiments, the compounds described herein inhibit TNAP. In certain embodiments, the compounds described herein are useful in the treatment of conditions associated with hyper- mineralization.

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