130627-10-0

• 

• Basic information

  1. Product Name: 2-AMINO-BENZOIC ACID 2-OXO-2-PHENYL-ETHYL ESTER
  2. Synonyms: 2-AMINO-BENZOIC ACID 2-OXO-2-PHENYL-ETHYL ESTER;2-OXO-2-PHENYLETHYL 2-AMINOBENZENECARBOXYLATE;2-Oxo-2-phenylethyl 2-aMinobenzoate
  3. CAS NO:130627-10-0
  4. Molecular Formula: C₁₅H₁₃NO₃
  5. Molecular Weight: 255.27
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 130627-10-0.mol
  9. Article Data: 8

• Chemical Properties

  1. Melting Point: 119-123°
  2. Boiling Point: 460.4°Cat760mmHg
  3. Flash Point: 231°C
  4. Appearance: /
  5. Density: 1.242g/cm³
  6. Vapor Pressure: 1.17E-08mmHg at 25°C
  7. Refractive Index: 1.616
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 2-AMINO-BENZOIC ACID 2-OXO-2-PHENYL-ETHYL ESTER(CAS DataBase Reference)
  11. NIST Chemistry Reference: 2-AMINO-BENZOIC ACID 2-OXO-2-PHENYL-ETHYL ESTER(130627-10-0)
  12. EPA Substance Registry System: 2-AMINO-BENZOIC ACID 2-OXO-2-PHENYL-ETHYL ESTER(130627-10-0)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: IRRITANT
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 130627-10-0(Hazardous Substances Data)

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• 2-OXO-2-PHENYLETHYL 2-AMINOBENZOATE

  Cas No: 130627-10-0

• USD $ 3.0-3.0 / Kilogram

• 1 Kilogram

• 1-100 Metric Ton/Month

• Dayang Chem (Hangzhou) Co.,Ltd.
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• Ethanone,2-[(2-aminobenzoyl)oxy]-1-phenyl-

  Cas No: 130627-10-0

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• Hangzhou J&H Chemical Co., Ltd.
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• 2-Oxo-2-phenylethyl 2-aminobenzenecarboxylate

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• Hunan chemfish Pharmaceutical co.,Ltd
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• 3-(4-Aminonaphthalen-1-yl)-N-Boc-L-alanine

  Cas No: 130627-10-0

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• Henan Allgreen Chemical Co.,Ltd
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• Ethanone,2-[(2-aminobenzoyl)oxy]-1-phenyl-

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• Henan Tianfu Chemical Co., Ltd.
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• 2-Oxo-2-phenylethyl 2-aminobenzenecarboxylate

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• 2-AMINO-BENZOIC ACID 2-OXO-2-PHENYL-ETHYL ESTER

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• 2-AMINO-BENZOIC ACID 2-OXO-2-PHENYL-ETHYL ESTER

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• Hangzhou Fandachem Co.,Ltd
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• 2-Oxo-2-phenylethyl 2-aminobenzenecarboxylate 130627-10-0

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• Hunan Russell Chemicals Technology Co.,Ltd
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• 2-Oxo-2-phenylethyl 2-aminobenzenecarboxylate 130627-10-0

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• Shenzhen Foris Technology Co. LTD
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130627-10-0 Usage

General Description

2-Amino-benzoic acid 2-oxo-2-phenyl-ethyl ester, also known as anthranilic acid benzyl ester, is a chemical compound with the molecular formula C15H13NO3. It is a white to off-white solid that is commonly used as an intermediate in the synthesis of organic compounds. 2-AMINO-BENZOIC ACID 2-OXO-2-PHENYL-ETHYL ESTER has a wide range of applications in the pharmaceutical, agrochemical, and dye industries. It is often used as a starting material for the production of various pharmaceuticals and agrochemicals due to its ability to react with a variety of organic compounds. Additionally, it is an important building block in the production of dyes and pigments, particularly in the synthesis of azo dyes. Overall, 2-amino-benzoic acid 2-oxo-2-phenyl-ethyl ester is a versatile compound with diverse applications in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 130627-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,6,2 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 130627-10:
(8*1)+(7*3)+(6*0)+(5*6)+(4*2)+(3*7)+(2*1)+(1*0)=90
90 % 10 = 0
So 130627-10-0 is a valid CAS Registry Number.

InChI:InChI=1/C15H13NO3/c16-13-9-5-4-8-12(13)15(18)19-10-14(17)11-6-2-1-3-7-11/h1-9H,10,16H2

130627-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name	phenacyl 2-aminobenzoate

1.2 Other means of identification

Product number	-
Other names	phenacyl anthranilate

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:130627-10-0 SDS

130627-10-0Upstream product

• 118-92-3 anthranilic acid 
• 70-11-1 α-bromoacetophenone 
• 552-16-9 ortho-nitrobenzoic acid 
• 55153-33-8 2-nitro-benzoic acid phenacyl ester 

130627-10-0Downstream Products

• 308832-66-8 2-hydroxymethyl-4-oxo-2-phenyl-1,2,3,4-tetrahydroquinazoline 
• 210489-25-1 4-Oxo-1,4-dihydro-quinoline-3,8-dicarboxylic acid 3-ethyl ester 8-(2-oxo-2-phenyl-ethyl) ester 
• 18543-22-1 2-benzoylaminobenzamide 
• 33809-77-7 2-acetamidobenzamide 
• 5398-63-0 2,5-diphenylpyrazine 
• 25827-94-5 2,6-diphenylpyrazine 
• 307330-37-6 2-oxo-2-phenylethyl 2-benzoylaminobenzoate 
• 461414-80-2 2-oxo-2-phenylethyl 2-acetylaminobenzoate 
• 210489-24-0 2-{[2-(2-Oxo-2-phenyl-ethoxycarbonyl)-phenylamino]-methylene}-malonic acid diethyl ester 

130627-10-0Relevant articles and documents

Solid-state induced heterocyclization under microwave irradiation: Synthesis of 2-phenyl-3-hydroxy-quinolin-4(1H)-one

Heravi, Majid M.,Oskooie, Hossein A.,Bahrami, Lila,Ghassemzadeh, Mitra

, p. 779 - 781 (2007/10/03)

Synthesis of 2-phenyl-3-hydroxy-quinolin-4(1H)-one under microwave irradiation in solventless system has been described. The mechanism of the reaction is also discussed.

2-Aryl-3-hydroxyquinolones, a new class of dyes with solvent dependent dual emission due to excited state intramolecular proton transfer

Yushchenko, Dmytro A.,Shvadchak, Volodymyr V.,Klymchenko, Andrey S.,Duportail, Guy,Mely, Yves,Pivovarenko, Vasyl G.

, p. 774 - 781 (2007/10/03)

Herein, the fluorescence properties of a series of 2-aryl-3- hydroxyquinolones (3HQs) were investigated and compared with the properties of well-studied 3-hydroxyflavone. All these compounds were found to display dual fluorescence with well-separated band

Synthetic Routes to 1,5-Dihydro-5-oxo-4,1-benzoxazepines and to 5-Oxooxazoloquinolines

Gandhi, Sham S.,Bell, Karen L.,Gibson, Martin S.

, p. 13301 - 13308 (2007/10/02)

The literature concerning phenacyl anthranilate, N-phenacylanthranilic acid and phenacyl N-phenacylanthranilate is clarified.Phenacyl anthranilate is dehydrated to 1,5-dihydro-5-oxo-2-phenyl-4,1-benzoxazepine by treatment with phosphoryl chloride; other examples of this reaction are described.A preparation of 4-methyl-5-oxo-2-phenyloxazoloquinoline from N-phenacylanthranilic acid and propionic anhydride is reported.

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