Cas 292824-85-2,<i>N</i>-[2-(4-chloro-but-2-enyloxy)-ethyl]-<i>N</i>-(2-hydroxy-ethyl)-4-methyl-benzenesulfonamide

292824-85-2

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Basic information

Product Name: N-[2-(4-chloro-but-2-enyloxy)-ethyl]-N-(2-hydroxy-ethyl)-4-methyl-benzenesulfonamide
Synonyms: N-[2-(4-chloro-but-2-enyloxy)-ethyl]-N-(2-hydroxy-ethyl)-4-methyl-benzenesulfonamide
CAS NO:292824-85-2
Molecular Formula:
Molecular Weight: 347.863
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-[2-(4-chloro-but-2-enyloxy)-ethyl]-N-(2-hydroxy-ethyl)-4-methyl-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[2-(4-chloro-but-2-enyloxy)-ethyl]-N-(2-hydroxy-ethyl)-4-methyl-benzenesulfonamide(292824-85-2)
EPA Substance Registry System: N-[2-(4-chloro-but-2-enyloxy)-ethyl]-N-(2-hydroxy-ethyl)-4-methyl-benzenesulfonamide(292824-85-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 292824-85-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 292824-85-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,2,8,2 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 292824-85:
(8*2)+(7*9)+(6*2)+(5*8)+(4*2)+(3*4)+(2*8)+(1*5)=172
172 % 10 = 2
So 292824-85-2 is a valid CAS Registry Number.

292824-85-2Upstream product

292824-85-2Downstream Products

292824-85-2Relevant academic research and scientific papers

Concise synthesis of azacycloundecenes using ring-closing metathesis (RCM)

Arisawa, Mitsuhiro,Kato, Chiaki,Kaneko, Hiroaki,Nishida, Atsushi,Nakagawa, Masako

, p. 1873 - 1876 (2007/10/03)

Azacycloundecenes, which are key intermediates in the synthesis of derivatives of the marine alkaloid manzamine C, are conveniently prepared using ring-closing olefin metathesis (RCM). The Royal Society of Chemistry 2000.

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