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2-Naphthaleneacetic acid, butyl ester, also known as NAA-butyl ester or butyl 2-naphthaleneacetate, is a synthetic plant growth regulator derived from the naturally occurring auxin hormone. It is a white crystalline solid with a molecular formula of C16H16O2 and a molecular weight of 240.30 g/mol. This chemical is widely used in agriculture to promote plant growth, root development, and fruit ripening. It is also employed in tissue culture techniques to stimulate cell division and elongation. The ester form of 2-naphthaleneacetic acid is more stable and less volatile than the free acid, making it easier to handle and apply. However, it is important to use this chemical responsibly, as it can have potential environmental and health impacts if not managed properly.

2876-68-8

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2876-68-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2876-68-8 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, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2876-68:
(6*2)+(5*8)+(4*7)+(3*6)+(2*6)+(1*8)=118
118 % 10 = 8
So 2876-68-8 is a valid CAS Registry Number.

2876-68-8SDS

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 butyl 2-naphthalen-2-ylacetate

1.2 Other means of identification

Product number -
Other names n-Butyl-2-naphthylacetat

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:2876-68-8 SDS

2876-68-8Downstream Products

2876-68-8Relevant academic research and scientific papers

Mono- and Bi-metallic Catalysed Formate-Halide Carbonylation Reactions

Buchan, Caroline,Hamel, Nathalie,Woell, James B.,Alper, Howard

, p. 167 - 168 (2007/10/02)

Benzylic, aryl, and alkyl halides react with formate esters and carbon monoxide, in the presence of the dimer of chloro(hexa-1,5-diene)rhodium(I), 2, to give carboxylic esters: bimetallic catalysis 2> is particularly beneficial when an aromatic halide is used as the substrate.

SYNTHESIS OF ESTERS BY RHODIUM(I) CATALYZED BORATE ESTER-BENZYLIC BROMIDE CARBONYLATION REACTIONS

Woell, James B.,Alper, Howard

, p. 3791 - 3794 (2007/10/02)

Benzylic halides react with trialkylborates and carbon monoxide, in the presence of 1,5-hexadienerhodium chloride dimer, to give esters in excellent yields.The reaction is applicable to the synthesis of primary, secondary and even tertiary esters.

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