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Benzoic acid, 2,6-bis(acetyloxy)-, also known as 2,6-diacetoxybenzoic acid, is an organic compound with the chemical formula C11H10O6. It is a derivative of benzoic acid, where two hydroxyl groups at the 2nd and 6th positions are replaced by acetyloxy groups. This white crystalline solid is used as a chemical intermediate in the synthesis of various pharmaceuticals, dyes, and other organic compounds. It is also known for its use in the preparation of certain esters and as a reagent in organic synthesis. The compound is typically synthesized through the acetylation of resorcinol or by the oxidation of 2,6-dihydroxyacetophenone.

3144-59-0

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3144-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3144-59-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,4 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3144-59:
(6*3)+(5*1)+(4*4)+(3*4)+(2*5)+(1*9)=70
70 % 10 = 0
So 3144-59-0 is a valid CAS Registry Number.

3144-59-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-diacetyloxybenzoic acid

1.2 Other means of identification

Product number -
Other names 2,6-diacetoxybenzoic acid

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:3144-59-0 SDS

3144-59-0Relevant academic research and scientific papers

O-glucosylated benzamide SGLT2 inhibitors and method

-

, (2008/06/13)

SGLT2 inhibiting compounds are provided having the formula wherein n is 0, 1 or 2; A is or heteroaryl which may contain 1 to 4 heteroatoms in the ring which may be selected from N, O, S, SO, and/or SO2, bearing substituents R3 and R4; and R1 to R4 are as defined herein. A method is also provided for treating diabetes and related diseases employing an SGLT2 inhibiting amount of the above compound alone or in combination with one, two or more other antidiabetic agents and/or one, two or more hypolipidemic agents.

Biological activity of the new herbicide LGC-40863 {benzophenone O-[2,6-bis[(4,6-dimethoxy-2-pyramdinyl)oxy]benzoyl]oxime}

Suk Jin Koo,Ahn,Jae Suk Lim,Sang Hern Chae,Jung Soo Kim,Jae Hwan Lee,Jin Ho Cho

, p. 109 - 114 (2007/10/03)

Herbicidal characteristics of the experimental compound LGC-40863 (ISO proposed common name: pyribenzoxim) were investigated in greenhouse and field. In the greenhouse, LGC-40863 had strong post-emergent activity on various grass and broadleaf weeds inclu

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