Cas 61706-01-2,4-chloro-N-[dimethyl(oxido)-lambda~6~-sulfanylidene]benzenesulfonamide

61706-01-2

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Basic information

Product Name: 4-chloro-N-[dimethyl(oxido)-lambda~6~-sulfanylidene]benzenesulfonamide
Synonyms: 4-Chloro-N-[dimethyl(oxido)-lambda~6~-sulfanylidene]benzenesulfonamide; Benzenesulfonamide, 4-chloro-N-(dimethyloxidosulfanylidene)-
CAS NO:61706-01-2
Molecular Formula: C₈H₁₀ClNO₃S₂
Molecular Weight: 267.7529
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: 405.8°C at 760 mmHg
Flash Point: 199.2°C
Appearance: N/A
Density: 1.42g/cm³
Vapor Pressure: 2E-06mmHg at 25°C
Refractive Index: 1.58
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-chloro-N-[dimethyl(oxido)-lambda~6~-sulfanylidene]benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-chloro-N-[dimethyl(oxido)-lambda~6~-sulfanylidene]benzenesulfonamide(61706-01-2)
EPA Substance Registry System: 4-chloro-N-[dimethyl(oxido)-lambda~6~-sulfanylidene]benzenesulfonamide(61706-01-2)

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: 61706-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 61706-01-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,0 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61706-01:
(7*6)+(6*1)+(5*7)+(4*0)+(3*6)+(2*0)+(1*1)=102
102 % 10 = 2
So 61706-01-2 is a valid CAS Registry Number.

61706-01-2Upstream product

52259-84-4 N-p-Chlorphenylsulfonyl-S,S-dimethyliminosulfuran

61706-01-2Downstream Products

61706-01-2Relevant academic research and scientific papers

PEROXYACETIC ACID: A USEFUL COOXIDANT FOR THE RUTHENIUM TETROXIDE OXIDATION OF N-SULFONYLSULFILIMINES

Ketcha, Daniel M.,Swern, Daniel

, p. 915 - 920 (2007/10/02)

The oxidation of a wide variety of N-sulfonylsulfilimines to the corresponding sulfoximines is described.The oxidation involves the use of peroxyacetic acid as a cooxidant for the actual oxidant, ruthenium tetroxide, in a biphasic media.

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