Cas 1236106-57-2,2-(phenylsulfonyl)-1',3'-dihydrospiro[1,3,2-dithiaphosphetane-4,2'-indene]2-sulfide

1236106-57-2

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Basic information

Product Name: 2-(phenylsulfonyl)-1',3'-dihydrospiro[1,3,2-dithiaphosphetane-4,2'-indene]2-sulfide
Synonyms: 2-(phenylsulfonyl)-1',3'-dihydrospiro[1,3,2-dithiaphosphetane-4,2'-indene]2-sulfide
CAS NO:1236106-57-2
Molecular Formula:
Molecular Weight: 352.506
EINECS: N/A
Product Categories: N/A
Mol File: 1236106-57-2.mol
Article Data: 1

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: 2-(phenylsulfonyl)-1',3'-dihydrospiro[1,3,2-dithiaphosphetane-4,2'-indene]2-sulfide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(phenylsulfonyl)-1',3'-dihydrospiro[1,3,2-dithiaphosphetane-4,2'-indene]2-sulfide(1236106-57-2)
EPA Substance Registry System: 2-(phenylsulfonyl)-1',3'-dihydrospiro[1,3,2-dithiaphosphetane-4,2'-indene]2-sulfide(1236106-57-2)

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: 1236106-57-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1236106-57-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,6,1,0 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1236106-57:
(9*1)+(8*2)+(7*3)+(6*6)+(5*1)+(4*0)+(3*6)+(2*5)+(1*7)=122
122 % 10 = 2
So 1236106-57-2 is a valid CAS Registry Number.

1236106-57-2Upstream product

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1236106-57-2Relevant articles and documents

Scope and limitation of the reaction of benzocycloalkanone oximes with lawesson′s reagents

Arsanious, Mona H. N.,Maigali, Soher S.,Boulos, Leila S.

experimental part, p. 57 - 64 (2010/05/02)

1,3,2,4-Dithiadiphosphetane-2,4-disulfide and its p-phenoxy derivatives react with 2-indanone-, 1-indanone-oxime, and tetralone oxime at different reaction temperatures to give 1,3,2-dithiaphosphetane-2-sulfide, dimeric compounds, 1-thioxo-1H-inden- phosp

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