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E-Hydroxyimino-phenylacetic acid, also known as E-HAPA, is an organic compound with the chemical formula C8H7NO3. It is a derivative of phenylacetic acid, featuring a hydroxyimino group (-OH-N=) attached to the phenyl ring. E-HYDROXYIMINO-PHENYLACETIC ACID is of interest in the field of organic chemistry and may have potential applications in the synthesis of various pharmaceuticals and chemical intermediates. E-HAPA is a chiral molecule, meaning it has non-superimposable mirror images, and it is typically synthesized through the reaction of phenylacetic acid with hydroxylamine. The compound's structure and properties make it a valuable building block in the development of new drugs and other chemical products.

704-18-7

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704-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 704-18-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 704-18:
(5*7)+(4*0)+(3*4)+(2*1)+(1*8)=57
57 % 10 = 7
So 704-18-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO3/c10-8(11)7(9-12)6-4-2-1-3-5-6/h1-5,12H,(H,10,11)/b9-7+

704-18-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E)-2-hydroxyimino-2-phenylacetic acid

1.2 Other means of identification

Product number -
Other names E-HYDROXYIMINO-PHENYLACETIC 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:704-18-7 SDS

704-18-7Relevant academic research and scientific papers

Tin(II) ketoacidoximates: Synthesis, X-ray structures and processing to tin(II) oxide

Khanderi, Jayaprakash,Davaasuren, Bambar,Alshankiti, Buthainah Ameen,Rothenberger, Alexander

, p. 19820 - 19828 (2015)

Tin(ii) ketoacidoximates of the type [HONCRCOO]2Sn (R = Me 1, CH2Ph 2) and (MeONCMeCOO)3Sn]- NH4+·2H2O 3 were synthesized by reacting pyruvate- and hydroxyl- or methoxylamine RONH2 (R = H, Me) with tin(ii) chloride dihydrate SnCl2·2H2O. The single crystal X-ray structure reveals that the geometry at the Sn atom is trigonal bipyramidal in 1, 2 and trigonal pyramidal in 3. Inter- or intramolecular hydrogen bonding is observed in 1-3. Thermogravimetric (TG) analysis shows that the decomposition of 1-3 to SnO occurs at ca. 160 °C. The evolved gas analysis during TG indicates complete loss of the oximato ligand in one step for 1 whereas a small organic residue is additionally removed at temperatures >400 °C for 2. Above 140 °C, [HONC(Me)COO]2Sn (1) decomposes in air to spherical SnO particles of size 10-500 nm. Spin coating of 1 on Si or a glass substrate followed by heating at 200 °C results in a uniform film of SnO. The band gap of the produced SnO film and nanomaterial was determined by diffuse reflectance spectroscopy to be in the range of 3.0-3.3 eV. X-ray photoelectron spectroscopy indicates surface oxidation of the SnO film to SnO2 in ambient atmosphere.

Synthesis of 2-Aminocarboxylic Acids on the Basis of Metalated Lithium Acylates

Zorin,Lenkova,Khachaturyan,Zorin

, p. 1590 - 1594 (2018/11/10)

2-Aminocarboxylic acids have been synthesized through the reaction of lithium acylate α-carbanions with alkyl nitrites to form α-hydroxyiminoacylates, followed by reduction of the latter with tin chloride. The reactions of lithium acylate α-carbanions, ge

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