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9H-Pyrido[3,4-b]indole, 3-[5-(ethylthio)-4-phenyl-4H-1,2,4-triazol-3-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105577-89-7

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105577-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105577-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,5,7 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 105577-89:
(8*1)+(7*0)+(6*5)+(5*5)+(4*7)+(3*7)+(2*8)+(1*9)=137
137 % 10 = 7
So 105577-89-7 is a valid CAS Registry Number.

105577-89-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-<2-N-phenyl-3-ethylmercapto-2,4,5-triazolyl>-9H-pyrido<3,4-b>indole

1.2 Other means of identification

Product number -
Other names 3-(5-Ethylsulfanyl-4-phenyl-4H-[1,2,4]triazol-3-yl)-9H-β-carboline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:105577-89-7 SDS

105577-89-7Relevant academic research and scientific papers

Studies on &β-Carbolines: Synthesis of 2-, 3- and 6-Substituted 9H-Pyridoindoles as Tubal Occluding Agents

Agarwal, Shiv K.,Saxena, Anil K.,Jain, Padam C.,Malviya, B.,Chandra, Harish,Anand, Nitya

, p. 757 - 760 (2007/10/02)

2-Substituted quaternary ammonium 9H-pyridoindole derivatives (2-4) have been obtained by the condensation of 9H-pyridoindole (1) with aminoalkyl chloride hydrochlorides. 3- and 6-Bromoacetamido-9H-pyridoindole hydrobromides (8/19) have been synthesized by the reaction of bromoacetyl bromide with corresponding 3-/6-amino-9H-pyridoindoles.The reaction of phenyl isothiocyanate on 9H-pyridoindole-3-carboxylic acid hydrazide (9) leads to the corresponding thiosemicarbazide (10), which on cyclisation with 4percent aq NaOH affords the triazine (11). 11 on reaction with C2H5I and ClCH2COOH affords ethyl mercaptotriazine (12) and carboxymethylmercaptotriazine (13) respectively.The ethylsulphonyltriazine (14) has been prepared by the oxidation of ethyl mercaptotriazine (11) while benzylidene derivative (15) has been obtained by condensation of C6H5CHO with hydrazide (9).Condensation of azide 16 with glycine furnishes 9H-pyridoindole-3-carbonylglycine (17).Compounds 1 and 11 produce 100 percent blockade in fallopian tubes of rhesus monkeys and mice respectively.

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