Cas 89982-42-3,1H-Phosphindole, 5,7-bis(1,1-dimethylethyl)-2,3-dihydro-1-mercapto-3,3-dimethyl-, 1-sulfide

89982-42-3

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Basic information

Product Name: 1H-Phosphindole, 5,7-bis(1,1-dimethylethyl)-2,3-dihydro-1-mercapto-3,3-dimethyl-, 1-sulfide
Synonyms:
CAS NO:89982-42-3
Molecular Formula: C18H29PS2
Molecular Weight: 340.534
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: 1H-Phosphindole, 5,7-bis(1,1-dimethylethyl)-2,3-dihydro-1-mercapto-3,3-dimethyl-, 1-sulfide(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Phosphindole, 5,7-bis(1,1-dimethylethyl)-2,3-dihydro-1-mercapto-3,3-dimethyl-, 1-sulfide(89982-42-3)
EPA Substance Registry System: 1H-Phosphindole, 5,7-bis(1,1-dimethylethyl)-2,3-dihydro-1-mercapto-3,3-dimethyl-, 1-sulfide(89982-42-3)

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: 89982-42-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 89982-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,8 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89982-42:
(7*8)+(6*9)+(5*9)+(4*8)+(3*2)+(2*4)+(1*2)=203
203 % 10 = 3
So 89982-42-3 is a valid CAS Registry Number.

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89982-42-3Relevant academic research and scientific papers

QUELQUES PROPRIETES CHIMIQUES DU TRIS(TERTIOBUTYL)-2,4,6 PHENYLDITHIOPHOSPHORANE

Navech, J.,Revel, M.,Kraemer, R.,Mathieu,S.

, p. 83 - 90 (2007/10/02)

The chemical properties of the dithiometaphosphonate analogue, tris(2,4,6-t-butyl)phenyldithiophosphorane (1), are reported in detail.

ETUDE DE LA REACTIVITE DU TRIS(TERTIOBUTYL)PHENYLDITHIOPHOSPHORANE

Navech, J.,Revel, M.,Kraemer, R.

, p. 207 - 210 (2007/10/02)

Heating of tris(tertiobutyl)phenyldithiophosphorane gives rise to an isomer with a tetracoordinated phosphorus atom.The action of triphenylphosphine loads to a tricyclophosphathiane which can be transformed in diphosphene by an excess of triphenylphosphine.Reactions with various nucleophilic derivatives (pyridine, triethylamine, diethylamine, butylamine, water, tetraphenylarsonium chloride) are described.

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