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Benzeneacetic acid, α-ethyl-, sodium salt, also known as Phenylethylsodium acetate or Sodium α-ethylbenzeneacetate, is an organic compound with the chemical formula C10H11NaO2. It is a sodium salt derived from benzeneacetic acid, featuring an ethyl group attached to the α-carbon. This white crystalline solid is soluble in water and is commonly used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Its properties include a melting point of 90-92°C and a density of 1.12 g/cm3. Due to its reactivity, it is typically handled with care in a controlled environment to prevent unwanted side reactions.

2686-71-7

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2686-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2686-71-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,8 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2686-71:
(6*2)+(5*6)+(4*8)+(3*6)+(2*7)+(1*1)=107
107 % 10 = 7
So 2686-71-7 is a valid CAS Registry Number.

2686-71-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium phenyl butyrate

1.2 Other means of identification

Product number -
Other names sodium phenylbutyrate

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:2686-71-7 SDS

2686-71-7Upstream product

2686-71-7Relevant academic research and scientific papers

Homo- and heteroleptic Zinc(II) carboxylates: Synthesis, structural characterization, and assessment of their biological significance in in vitro models

Ali, Saqib,Bibi, Memoona,Faisal, Sulaiman,Gul, Amna,Haider, Ali,Nadhman, Akhtar,Naz, Saba,Uddin, Noor,Ullah, Kaleem,Yousuf, Sammer

, (2020)

A series of five new zinc(II) complexes of 2-phenylbutyric acid comprising of one homoleptic (1) and four heteroleptic (2–5) complexes were synthesized under open beaker conditions. The behavior of the complexes in the solid and solution state was explored through FT-IR and NMR (1H and 13C) spectroscopy, respectively. Crystallographic data have revealed that complexes 2 and 3 crystallized in monoclinic and triclinic crystal system, respectively, with a distorted octahedral geometry, whereas complex 4 crystallized in monoclinic crystal system with a pentagonal geometry around the zinc(II) atom. All the complexes have been screened for enzyme (alkaline phosphatase) inhibition, in vitro hemolysis and antileishmanial activity, DNA and cetyltrimethylammonium bromide (CTAB) interaction. The increase in the concentration of complexes 1, 2, 4 and 5 remarkably decreases the activity of enzyme alkaline phosphatase, whereas complex 3 was found inactive. The behavior of the complexes as a potent drug is clear from the results of hemolysis and antileishmanial activity against promastigote. The UV–Vis spectroscopic data of complexes–DNA interactions suggested a surface binding mode whereas the interaction of CTAB with complexes, studied through conductometry, confirmed strong interacting ability of complexes with CTAB.

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