Cas 6392-05-8,4-[(4-methoxy-phenyl)-methylsulfanyl-methylene]-morpholinium; iodide

6392-05-8

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Basic information

Product Name: 4-[(4-methoxy-phenyl)-methylsulfanyl-methylene]-morpholinium; iodide
Synonyms: 4-[(4-methoxy-phenyl)-methylsulfanyl-methylene]-morpholinium; iodide
CAS NO:6392-05-8
Molecular Formula:
Molecular Weight: 379.262
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: 4-[(4-methoxy-phenyl)-methylsulfanyl-methylene]-morpholinium; iodide(CAS DataBase Reference)
NIST Chemistry Reference: 4-[(4-methoxy-phenyl)-methylsulfanyl-methylene]-morpholinium; iodide(6392-05-8)
EPA Substance Registry System: 4-[(4-methoxy-phenyl)-methylsulfanyl-methylene]-morpholinium; iodide(6392-05-8)

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: 6392-05-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 6392-05-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,9 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6392-05:
(6*6)+(5*3)+(4*9)+(3*2)+(2*0)+(1*5)=98
98 % 10 = 8
So 6392-05-8 is a valid CAS Registry Number.

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6392-05-8Downstream Products

6392-05-8Relevant academic research and scientific papers

HIGHLY COORDINATE ORGANOSILICON COMPOUNDS IN SYNTHESIS: NEW ENTRY TO S,N-ACETALS BY SELECTIVE REDUCTION OF ALKYLTHIOMETHYLENIMINIUM SALTS BY USE OF TRIMETHOXYSILANE AND DILITHIUM 2,3-BUTANDIOLATE

Tominaga, Yoshinori,Matsuoka, Yoshiki,Hayashida, Hisashi,Kohra, Shinya,Hosomi, Akira

, p. 5771 - 5774 (2007/10/02)

Reduction of alkylthiomethyleniminium iodides proceeds smoothly by use of trimethoxysilane and dilithium 2,3-butandiolate in tetrahydrofuran at 0 deg C to give the corresponding S,N-acetals selectively in high yield.

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