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93100-99-3

93100-99-3

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93100-99-3 Usage

Description

W-15 (Item No. 14898) is an analytical reference material categorized as an analgesic. This product is intended for research and forensic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 93100-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,0 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 93100-99:
(7*9)+(6*3)+(5*1)+(4*0)+(3*0)+(2*9)+(1*9)=113
113 % 10 = 3
So 93100-99-3 is a valid CAS Registry Number.
InChI:InChI=1S/C19H21ClN2O2S/c20-17-9-11-18(12-10-17)25(23,24)21-19-8-4-5-14-22(19)15-13-16-6-2-1-3-7-16/h1-3,6-7,9-12H,4-5,8,13-15H2/b21-19-

93100-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (NZ)-4-chloro-N-[1-(2-phenylethyl)piperidin-2-ylidene]benzenesulfonamide

1.2 Other means of identification

Product number -
Other names QC-620

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:93100-99-3 SDS

93100-99-3Relevant articles and documents

Some Reactions of 1-Methyl-(2-phenylethyl)-1,2,3,4-tetrahydropyridines with Organic Azides. Synthesis of 1-Methyl-(2-phenylethyl)piperidylidene-2-sulfonamides

Warren, Brent K.,Knaus, Edward E.

, p. 1413 - 1416 (2007/10/02)

The 1,3-dipolar cycloaddition reaction of 1-methyl- and 1-(2-phenylethyl)-1,2,3,4-tetrahydropyridines 7 with organic azides 8 afforded the respective 1-substituted-piperidylidene-2-sulfon(cyan)amides 9.Nitration of the 1-(2-phenylethyl) analogue 9o yielded the 1- derivative 9r which on reduction with palladium-on-charcoal and hydrazine gave the 1- analogue 9s.