19077-78-2 Usage
Description
Methyl 4-chloroindolyl-3-acetate, also known as 4-chloroindole-3-acetic acid methyl ester, is a chemical compound derived from the indole alkaloid family. It is characterized by its unique chemical structure, which includes a chlorine atom at the 4-position and an acetate group at the 3-position. methyl 4-chloroindolyl-3-acetate has potential applications in various fields due to its distinct properties and reactivity.
Uses
Used in Biological Studies:
Methyl 4-chloroindolyl-3-acetate is used as a biological study agent for investigating the metabolism and bioactivity of 4-chloroindole-3-acetic acid in plants. It helps researchers understand the role and behavior of this compound within the plant system, which can be crucial for developing new strategies in plant biology and agriculture.
Used in Mass Spectrometry:
Methyl 4-chloroindolyl-3-acetate is also used as a reagent or reactant in the field of mass spectrometry. It aids in the interpretation of mass spectral characteristic fragmentation mechanisms of indole alkaloids. By determining the initial ionization site, researchers can gain valuable insights into the structural and chemical properties of these complex molecules, which can be applied in various scientific and industrial applications.
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
19077-78-2Relevant 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.