Cas 76345-29-4,N-[1-Cyclohexylamino-1-ethylamino-meth-(E)-ylidene]-4-methyl-benzenesulfonamide

76345-29-4

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Basic information

Product Name: N-[1-Cyclohexylamino-1-ethylamino-meth-(E)-ylidene]-4-methyl-benzenesulfonamide
Synonyms: N-[1-Cyclohexylamino-1-ethylamino-meth-(E)-ylidene]-4-methyl-benzenesulfonamide
CAS NO:76345-29-4
Molecular Formula:
Molecular Weight: 323.459
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: N-[1-Cyclohexylamino-1-ethylamino-meth-(E)-ylidene]-4-methyl-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[1-Cyclohexylamino-1-ethylamino-meth-(E)-ylidene]-4-methyl-benzenesulfonamide(76345-29-4)
EPA Substance Registry System: N-[1-Cyclohexylamino-1-ethylamino-meth-(E)-ylidene]-4-methyl-benzenesulfonamide(76345-29-4)

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: 76345-29-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 76345-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,4 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76345-29:
(7*7)+(6*6)+(5*3)+(4*4)+(3*5)+(2*2)+(1*9)=144
144 % 10 = 4
So 76345-29-4 is a valid CAS Registry Number.

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76345-29-4Relevant academic research and scientific papers

Thione S-Imide. Reaction with Heterocumulenes

Saito, Takao,Oikawa, Isao,Motoki, Shinichi

, p. 2582 - 2585 (1980)

9-Fluorenethione S-p-toluenesulfonimide reacted with diphenylketene to give two regioisomeric 1,3-dipolar cycloadducts.The thione S-imide and symmetrical dialkylcarbodiimides produced 3-tosylimino-1,2,4-thiadiazolidines.In the reaction with ketenimines, there occurred siteselective cycloaddition reactions on C=N vs.C=C bonds in the imines and further rearrangement of the 1,2,4-thiadiazolidine adducts.

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