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54648-89-4

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54648-89-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54648-89-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,4 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54648-89:
(7*5)+(6*4)+(5*6)+(4*4)+(3*8)+(2*8)+(1*9)=154
154 % 10 = 4
So 54648-89-4 is a valid CAS Registry Number.

54648-89-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[[2-(2-methyl-1H-indol-3-yl)acetyl]amino]-3-phenylthiourea

1.2 Other means of identification

Product number -
Other names -

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:54648-89-4 SDS

54648-89-4Relevant articles and documents

Synthesis, lipophilicity and biological evaluation of indole-containing derivatives of 1,3,4-thiadiazole and 1,2,4-triazole

Varvaresou, Athanasia,Siatra-Papastaikoudi, Theodora,Tsotinis, Andrew,Tsantili-Kakoulidou, Anna,Vamvakides, Alexandre

, p. 320 - 326 (1998)

3-[(2-Methyl-1H-3-indolyl)methyl]-4-aryl-4,5-dihydro-1H-1,2,4-triazole- 5-thiones 6a-c and their respective N-{5-[(2-methyl-1H-3-indolyl) methyl] - 1,3,4-thiadiazol-2-yl }-N-arylamines 7a,b have been prepared. The antidepressant profile of 6a,c and 7a was

Synthesis of Some Indole Derivatives as Potential Antibacterial Agents

Sengupta, Anil K.,Gupta, Anurag Ateet

, p. 263 - 266 (2007/10/02)

Thiosemicarbazides (III), ureas (V), triazoles (VI) and organotin compounds (VII) having 2-alkylindole as a common structural feature have been synthesized and their antibacterial activity has been evaluated against Bacillus subtilis, Bacillus pumilus, St

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