Cas 76924-22-6,N-BUTYL-N-(1,1-DIOXIDOTETRAHYDROTHIEN-3-YL)AMINE HYDROCHLORIDE

76924-22-6

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Basic information

Product Name: N-BUTYL-N-(1,1-DIOXIDOTETRAHYDROTHIEN-3-YL)AMINE HYDROCHLORIDE
Synonyms: N-BUTYL-N-(1,1-DIOXIDOTETRAHYDROTHIEN-3-YL)AMINE HYDROCHLORIDE
CAS NO:76924-22-6
Molecular Formula: C8H18ClNO2S
Molecular Weight: 227.75
EINECS: N/A
Product Categories: N/A
Mol File: 76924-22-6.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-BUTYL-N-(1,1-DIOXIDOTETRAHYDROTHIEN-3-YL)AMINE HYDROCHLORIDE(CAS DataBase Reference)
NIST Chemistry Reference: N-BUTYL-N-(1,1-DIOXIDOTETRAHYDROTHIEN-3-YL)AMINE HYDROCHLORIDE(76924-22-6)
EPA Substance Registry System: N-BUTYL-N-(1,1-DIOXIDOTETRAHYDROTHIEN-3-YL)AMINE HYDROCHLORIDE(76924-22-6)

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: 76924-22-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 76924-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,2 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76924-22:
(7*7)+(6*6)+(5*9)+(4*2)+(3*4)+(2*2)+(1*2)=156
156 % 10 = 6
So 76924-22-6 is a valid CAS Registry Number.

76924-22-6Upstream product

76924-18-0 1,1-dioxo-3-thiolanyl butylcarbamate

76924-22-6Downstream Products

76924-22-6Relevant academic research and scientific papers

HYDROLYSIS OF CARBAMATES AND CARBONATES OF 3-HYDROXYTHIOLANE 1,1-DIOXIDE

Parkhomenko, P. I.,Rybakova, M. V.,Bezmenova, T. E.,Zaika, T. D.

, p. 1122 - 1124 (1980)

Alkylcarbamates of 3-hydroxy-thiolane 1,1-dioxide are hydrolyzed in the presence of bases to give alkyl(1,1-dioxo-3-thiolanyl)amines and 2-thiolene 1,1-dioxide (I).Aryl esters undergo hydrolysis to give sulfone I and 3-hydroxythiolane 1,1-dioxide (II).The corresponding alkyl- and arylcarbonates also form sulfone I and a very small amount of hydroxy derivative II under these conditions.

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