Cas 767-65-7,BENZO[1,2,5]SELENADIAZOL-4-YLAMINE

767-65-7

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Basic information

Product Name: BENZO[1,2,5]SELENADIAZOL-4-YLAMINE
Synonyms: BENZO[1,2,5]SELENADIAZOL-4-YLAMINE;ZERENEX E/4039357
CAS NO:767-65-7
Molecular Formula: C6H5N3Se
Molecular Weight: 198.08
EINECS: N/A
Product Categories: N/A
Mol File: 767-65-7.mol

Chemical Properties

Melting Point: 159.5-160.5 °C
Boiling Point: 346.9±34.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 0.85±0.10(Predicted)
CAS DataBase Reference: BENZO[1,2,5]SELENADIAZOL-4-YLAMINE(CAS DataBase Reference)
NIST Chemistry Reference: BENZO[1,2,5]SELENADIAZOL-4-YLAMINE(767-65-7)
EPA Substance Registry System: BENZO[1,2,5]SELENADIAZOL-4-YLAMINE(767-65-7)

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: 767-65-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 767-65-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 767-65:
(5*7)+(4*6)+(3*7)+(2*6)+(1*5)=97
97 % 10 = 7
So 767-65-7 is a valid CAS Registry Number.

767-65-7Upstream product

767-65-7Downstream Products

767-65-7Relevant academic research and scientific papers

(AZA)INDOLE-, BENZOTHIOPHENE-, AND BENZOFURAN-3-SULFONAMIDES

-

, (2018/07/29)

Disclosed are sulfonamide compounds with GPR17 modulating properties, which are useful for treating or preventing a variety of CNS and other diseases, in particular for preventing and treating myelinating diseases or disorders.

Application of the Gould-Jacobs reaction to 4-amino-2,1,3- benzoselenadiazole

Bella, Maro,Schultz, Marcel,Milata, Viktor,Koariková, Katarína,Breza, Martin

experimental part, p. 8169 - 8174 (2010/11/18)

An effective method for the synthesis of 4-amino-2,1,3-benzoselenadiazole (4) has been described. Reduction of readily available 4-nitrobenzothiadiazole 6 with SnCl2·2H2O afforded 1,2,3-triaminobenzene dihydrochloride 2. The latter u

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