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19077-78-2

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19077-78-2 Usage

Uses

4-Chloroindole-3-acetic Acid Methyl Ester can be used in biological study for metabolism and bioactivity of 4-chloroindole-3-acetic acid in plants. It can also be used as reagent/reactant for interpretation of mass spectral characteristic fragmentation mechanisms of indole alkaloids through determining initial ionization site.

Check Digit Verification of cas no

The CAS Registry Mumber 19077-78-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,7 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19077-78:
(7*1)+(6*9)+(5*0)+(4*7)+(3*7)+(2*7)+(1*8)=132
132 % 10 = 2
So 19077-78-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H10ClNO2/c1-15-10(14)5-7-6-13-9-4-2-3-8(12)11(7)9/h2-4,6,13H,5H2,1H3

19077-78-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(4-chloro-1H-indol-3-yl)acetate

1.2 Other means of identification

Product number -
Other names Methyl 4-chloroindolyl-3-acetate

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:19077-78-2 SDS

19077-78-2Relevant articles and documents

Synthesis and biological activities of 4-chloroindole-3-acetic acid and its esters.

Katayama

, p. 808 - 815 (2007/10/03)

4-Chloroindole-3-acetic acid (4-Cl-IAA) and its esters were synthesized from 2-chloro-6-nitrotoluene as the starting material. The biological activities of 4-CI-IAA and its esters were determined by four bioassays. Except for the tert-butyl ester, 4-Cl-IAA and its esters had stronger elongation activity toward Avena coleoptiles than had indole-3-acetic acid. The biological activities of the methyl, ethyl and allyl esters were as strong as the activity of the free acid. All the esters, except for the tert-butyl, inhibited Chinese cabbage hypocotyl growth more than the free acid did, and all the esters induced severe swelling and formation of numerous lateral roots in black gram seedlings even at a low concentration. Furthermore, adventitious root formation was strongly promoted in Serissa japonica cuttings by all the esters. The root formation-promoting activities of the ethyl and allyl esters were about three times the value for indole-3-butyric acid which is used to promote and accelerate root formation in plant cuttings.

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