Cas 102104-98-3,N-(6-methylbenzyl<5,6>cyclohepta<1,2-a>pyridin-11-ylidene)-3-nitrobenzenesulfenamide

102104-98-3

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Basic information

Product Name: N-(6-methylbenzyl<5,6>cyclohepta<1,2-a>pyridin-11-ylidene)-3-nitrobenzenesulfenamide
Synonyms:
CAS NO:102104-98-3
Molecular Formula:
Molecular Weight: 373.435
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-(6-methylbenzyl<5,6>cyclohepta<1,2-a>pyridin-11-ylidene)-3-nitrobenzenesulfenamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(6-methylbenzyl<5,6>cyclohepta<1,2-a>pyridin-11-ylidene)-3-nitrobenzenesulfenamide(102104-98-3)
EPA Substance Registry System: N-(6-methylbenzyl<5,6>cyclohepta<1,2-a>pyridin-11-ylidene)-3-nitrobenzenesulfenamide(102104-98-3)

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: 102104-98-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 102104-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,1,0 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 102104-98:
(8*1)+(7*0)+(6*2)+(5*1)+(4*0)+(3*4)+(2*9)+(1*8)=63
63 % 10 = 3
So 102104-98-3 is a valid CAS Registry Number.

102104-98-3Upstream product

72694-64-5 6-methylbenzo<5,6>cyclohepta<1,2-c>pyridin-11-one

102104-98-3Downstream Products

102104-98-3Relevant academic research and scientific papers

Imino-Bridged Heterocycles. IV . A Facile Synthesis of Sulfenimines Derived from Diaryl Ketones

Brenner, Daniel G.,Cavolowsky, Kathleen Mensler,Shepard, Kenneth L.

, p. 805 - 808 (2007/10/02)

Efficient, high-yield syntheses of N-diarylmethylene sulfenamides (sulfenimines) have been developed under mild laboratory conditions.Diaryl ketones have been shown to form ketimines readily by condensation with ammonia in the presence of titanium tetrachloride.

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