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2876-71-3

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2876-71-3 Usage

General Description

Beta-Naphthylacetic acid, methyl ester is a chemical compound that is derived from naphthalene and is commonly used as a plant growth regulator. It acts as a synthetic auxin, a class of plant hormones that promote cell elongation and division, and is therefore used to stimulate root formation, enhance fruit set, and increase yield in various crops. It is often applied as a foliar spray or as a dip for cuttings and has been found to be effective in promoting root growth in a variety of plant species. As a synthetic growth regulator, Beta-Naphthylacetic acid, methyl ester is an important tool for the agricultural industry in managing plant growth and productivity.

Check Digit Verification of cas no

The CAS Registry Mumber 2876-71-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,7 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2876-71:
(6*2)+(5*8)+(4*7)+(3*6)+(2*7)+(1*1)=113
113 % 10 = 3
So 2876-71-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H12O2/c1-15-13(14)9-10-6-7-11-4-2-3-5-12(11)8-10/h2-8H,9H2,1H3

2876-71-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name β-Naphthylacetic acid,methyl ester

1.2 Other means of identification

Product number -
Other names 2-Naphthaleneacetic acid methyl ester

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:2876-71-3 SDS

2876-71-3Relevant articles and documents

Catalytic Carboxylation of Heteroaromatic Compounds: Double and Single Carboxylation with CO 2

Mita, Tsuyoshi,Masutani, Hiroki,Ishii, Sho,Sato, Yoshihiro

supporting information, p. 841 - 845 (2019/04/25)

In the presence of PdCl 2 [P(n -Bu) 3 ] 2 (10 mol%) and ZnEt 2, 2-furyl and 2-pyrrolylmethyl acetate were carboxylated with CO 2 (1 atm), affording doubly carboxylated products in good yields. In this dearomative transformation, α,?-dicarboxylic acids were obtained selectively, in contrast to our previous report in which α,γ-dicarboxylic acids were selectively produced from 2-indolylmethyl acetates. In contrast, 5-thiazolylmethyl acetate and naphthylmethyl acetates predominantly underwent single carboxylation.

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