Welcome to LookChem.com Sign In|Join Free

CAS

  • or
Methyl 2-[(phenylcarbamoyl)amino]benzoate is a chemical compound with the molecular formula C15H14N2O3. It is an organic ester derived from benzoic acid, where the carboxylic acid group is esterified with methanol, and the amino group is part of a phenylcarbamoyl moiety. methyl 2-[(phenylcarbamoyl)amino]benzoate is characterized by its aromatic structure, featuring a benzene ring with a carbamate group attached to the 2-position, which is further connected to another benzene ring through an amide linkage. It is a white crystalline solid and is used in the synthesis of various pharmaceuticals and chemical intermediates due to its unique structural properties.

2321-50-8 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 2321-50-8 Structure
  • Basic information

    1. Product Name: methyl 2-[(phenylcarbamoyl)amino]benzoate
    2. Synonyms: Benzoic acid, 2-[[(phenylamino)carbonyl]amino]-, methyl ester; Methyl 2-[(phenylcarbamoyl)amino]benzoate
    3. CAS NO:2321-50-8
    4. Molecular Formula: C15H14N2O3
    5. Molecular Weight: 270.2833
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2321-50-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 337°C at 760 mmHg
    3. Flash Point: 157.6°C
    4. Appearance: N/A
    5. Density: 1.3g/cm3
    6. Vapor Pressure: 0.000108mmHg at 25°C
    7. Refractive Index: 1.661
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: methyl 2-[(phenylcarbamoyl)amino]benzoate(CAS DataBase Reference)
    11. NIST Chemistry Reference: methyl 2-[(phenylcarbamoyl)amino]benzoate(2321-50-8)
    12. EPA Substance Registry System: methyl 2-[(phenylcarbamoyl)amino]benzoate(2321-50-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2321-50-8(Hazardous Substances Data)

2321-50-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2321-50-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,2 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2321-50:
(6*2)+(5*3)+(4*2)+(3*1)+(2*5)+(1*0)=48
48 % 10 = 8
So 2321-50-8 is a valid CAS Registry Number.

2321-50-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(phenylcarbamoylamino)benzoate

1.2 Other means of identification

Product number -
Other names N-phenylcarbamoyl-anthranilic acid methyl ester

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:2321-50-8 SDS

2321-50-8Relevant articles and documents

COMPOUNDS AND METHODS FOR INDUCING CHONDROGENESIS

-

Paragraph 0775; 0777; 0786, (2014/09/29)

Described herein are compounds and compositions for the amelioration of arthritis or joint injuries by inducing mesenchymal stem cells into chondrocytes.

3-aryl(alkyl)quinazoline-2,4(1H,3H)-diones and their alkyl derivatives

Shestakov,Sidorenko,Bushmarinov,Shikhaliev,Antipin

experimental part, p. 1691 - 1696 (2010/04/29)

Two-stage reaction of methyl anthranilate with aryl(alkyl) isocyanates in keeping with the quantumchemical calculations and XRD analysis resulted in 3-aryl(alkyl)quinazoline-2,4(1H,3H)-diones that by treatment with alkyl halides, phenacyl bromides, esters

Progesterone receptor antagonists with a 3-phenylquinazoline-2,4-dione/2-phenylisoquinoline-1,3-dione skeleton

Nakagawa, Aya,Uno, Shigeyuki,Makishima, Makoto,Miyachi, Hiroyuki,Hashimoto, Yuichi

, p. 7046 - 7054 (2008/12/22)

Novel non-steroidal progesterone receptor antagonists with a 3-phenylquinazoline-2,4-dione/2-phenylisoquinoline-1,3-dione skeleton were developed and their structure-activity relationships were investigated. Among the prepared compounds, 4-(4,4-diethyl-3,

Microwave promoted solvent-free one-pot synthesis of N,N′- disubstituted urea derivatives

Jadhav, Vinod H.,Deshpande, Shubhada S.,Borate, Hanumant B.,Wakharkar, Radhika D.

, p. 205 - 208 (2007/10/03)

An efficient one-pot synthesis of N,N′-disubstituted urea derivatives from substituted anilines, ethyl chloroformate and methyl anthranilate or methyl 3-amino-2-butenoate under microwave irradiation is reported.

Specific nonpeptide inhibitors of puromycin-sensitive aminopeptidase with a 2,4(1H,3H)-quinazolinedione skeleton.

Kakuta, Hiroki,Tanatani, Aya,Nagasawa, Kazuo,Hashimoto, Yuichi

, p. 1273 - 1282 (2007/10/03)

Potent, specific, chemically stable and non-peptide/small-molecular inhibitors of puromycin-sensitive aminopeptidase, such as 3-(2,6-diethylphenyl)-2,4(1H,3H)-quinazolinedione (PAQ-22, 5), were prepared by the structural development of a potent PSA inhibitor, 2-(2,6-diethylphenyl)-1,2,3,4-tetrahydroisoquinoline-1,3-dione (PIQ-22, 4). The design was carried out partly by applying electrostatic potential field information obtained from PIQ-22 (4) and its derivatives based on thalidomide (2). This information revealed that a positive electrostatic potential field around the benzylic methylene in the tetrahydroisoquinoline ring is necessary for potent activity. Lineweaver-Burk plot analysis showed that PAQ-22 (5) and its derivatives inhibit puromycin-sensitive aminopeptidase (PSA) in a non-competitive manner. These potent and specific PSA inhibitors showed dose-dependent cell invasion-inhibitory activity in a Matrigel assay using mouse melanoma B16F10/L5 cells, in spite of their low cell toxicity.

Convenient Preparation of N-substituted 2-Amino-4H-3,1-benzoxazin-4-ones and 3-Substituted 2,4(1H,3H)-Quinazolinediones

Papadopoulos, E. P.,Torres, C. D.

, p. 269 - 272 (2007/10/02)

Room temperature of 2-(3-arylureido)benzoic acids (1) and methyl2-(3-alkyl-, or 3-arylureido)-benzoates (2) with concentrated sulfuric acid leads to N-substituted 2-amino-4H-3,1-benzoxazin-4-ones (3) in generally very good yields.The isomeric 3-substitute

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 2321-50-8