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1H-Indole-1-carboxylic acid, 4-hydroxy-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75201-79-5

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75201-79-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75201-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,0 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75201-79:
(7*7)+(6*5)+(5*2)+(4*0)+(3*1)+(2*7)+(1*9)=115
115 % 10 = 5
So 75201-79-5 is a valid CAS Registry Number.

75201-79-5SDS

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 benzyl 4-hydroxyindole-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-benzyloxycarbonyl-4-hydroxyindole

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:75201-79-5 SDS

75201-79-5Relevant academic research and scientific papers

Anionically substituted 7-Nitroindoline derivatives and their uses

-

Page/Page column 8; 12, (2010/11/25)

Anionically substituted 7-nitroindoline derivatives are disclosed and their uses as caged compounds from which effector species such as neurotransmitters and amino acids are releasable on irradiation with light.

A strategy to avoid anomalous O-alkylation of 4-hydroxyindole by diethyl bromomalonate

Papageorgiou, George,Corrie, John E. T.

, p. 1101 - 1104 (2007/10/03)

Alkylation of 4-hydroxyindole with diethyl bromomalonate under standard conditions (potassium carbonate-acetone) gave the expected indolyloxymalonate ester 3 together with the anomalous indolyloxy-2-bromomalonate 4, Depending on conditions, the ratio of t

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