Cas 2800-78-4,1-(4-amino-benzenesulfonyl)-3-cyclohexyl-2-methyl-isothiourea

2800-78-4

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Basic information

Product Name: 1-(4-amino-benzenesulfonyl)-3-cyclohexyl-2-methyl-isothiourea
Synonyms: 1-(4-amino-benzenesulfonyl)-3-cyclohexyl-2-methyl-isothiourea
CAS NO:2800-78-4
Molecular Formula:
Molecular Weight: 327.472
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: 1-(4-amino-benzenesulfonyl)-3-cyclohexyl-2-methyl-isothiourea(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-amino-benzenesulfonyl)-3-cyclohexyl-2-methyl-isothiourea(2800-78-4)
EPA Substance Registry System: 1-(4-amino-benzenesulfonyl)-3-cyclohexyl-2-methyl-isothiourea(2800-78-4)

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: 2800-78-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 2800-78-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2800-78:
(6*2)+(5*8)+(4*0)+(3*0)+(2*7)+(1*8)=74
74 % 10 = 4
So 2800-78-4 is a valid CAS Registry Number.

2800-78-4Upstream product

2800-78-4Downstream Products

2651-24-3 N-(4-amino-benzenesulfonyl)-morpholine 4-carboximidic acid cyclohexylamide

2800-78-4Relevant academic research and scientific papers

Synthesis and bactericidal activity of some symmetrical bisthioalkyl derivatives

Seshadri, S.,Sanghavi, N. M.,Naik, R. V.,Tawate, S. R.,Trivedi, M. N.,Fruitwala, M. A.

, p. 688 - 692 (2007/10/02)

The paper deals with the synthesis of some bactericides.The dithioacetal required are obtained by the reaction of active methylene compounds and aryl sulphonamides with carbon disulphide in alkaline conditions and subsequent alkylation with dimethyl sulphate.These compounds are then reacted with various pharmacopohores.All the compounds show moderate to significant activity with few compounds showing very high broad spectrum activity.

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