Cas 219126-59-7,[3-(Benzothiazol-2-ylsulfanyl)-2-methyl-propyl]-trityl-amine

219126-59-7

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Basic information

Product Name: [3-(Benzothiazol-2-ylsulfanyl)-2-methyl-propyl]-trityl-amine
Synonyms: [3-(Benzothiazol-2-ylsulfanyl)-2-methyl-propyl]-trityl-amine
CAS NO:219126-59-7
Molecular Formula:
Molecular Weight: 480.698
EINECS: N/A
Product Categories: N/A
Mol File: 219126-59-7.mol
Article Data: 1

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: [3-(Benzothiazol-2-ylsulfanyl)-2-methyl-propyl]-trityl-amine(CAS DataBase Reference)
NIST Chemistry Reference: [3-(Benzothiazol-2-ylsulfanyl)-2-methyl-propyl]-trityl-amine(219126-59-7)
EPA Substance Registry System: [3-(Benzothiazol-2-ylsulfanyl)-2-methyl-propyl]-trityl-amine(219126-59-7)

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: 219126-59-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 219126-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,1,2 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 219126-59:
(8*2)+(7*1)+(6*9)+(5*1)+(4*2)+(3*6)+(2*5)+(1*9)=127
127 % 10 = 7
So 219126-59-7 is a valid CAS Registry Number.

219126-59-7Upstream product

120-78-5 di(benzothiazol-2-yl)disulfide

219126-59-7Downstream Products

219126-59-7Relevant articles and documents

Synthesis of a series of sulfinic acid analogs of GABA and evaluation of their GABA(B) receptor affinities

Carruthers, Nicholas I.,Spitler, James M.,Wong, Shing-Chun,Blythin, David J.,Chen, Xiao,Shue, Ho-Jane,She, Hoyan S.,Lee, Joe F.,Rizzo, Charles,Ting, Pauline C.,West Jr., Robert E.

, p. 3059 - 3064 (1998)

A series of γ-aminobutyric acid (GABA) 1 analogs was prepared in which the carboxylic acid group of GABA was replaced with a sulfinic acid group and their affinity for the GABA(B) receptor investigated.

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