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BENZHYDRYLAMINOACETIC ACID, TERT-BUTYL ESTER is a light brown crystalline solid that serves as a valuable intermediate in the synthesis of 2-Azetidinones, which are important compounds in the pharmaceutical industry.

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  • 158980-46-2 Structure
  • Basic information

    1. Product Name: BENZHYDRYLAMINOACETIC ACID, TERT-BUTYL ESTER
    2. Synonyms: BENZHYDRYLAMINOACETIC ACID, TERT-BUTYL ESTER;TERT-BUTYL(DIPHENYLMETHYLAMINO)ETHANOATE;N-(Diphenylmethyl)glycine 1,1-Dimethylethyl Ester
    3. CAS NO:158980-46-2
    4. Molecular Formula: C19H23NO2
    5. Molecular Weight: 297.39
    6. EINECS: N/A
    7. Product Categories: Amino Acids 13C, 2H, 15N;Amino Acids & Derivatives;Aromatics;Intermediates
    8. Mol File: 158980-46-2.mol
  • Chemical Properties

    1. Melting Point: 75.5-76.5°C
    2. Boiling Point: 393.745 °C at 760 mmHg
    3. Flash Point: 191.93 °C
    4. Appearance: /
    5. Density: 1.058 g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.544
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: BENZHYDRYLAMINOACETIC ACID, TERT-BUTYL ESTER(CAS DataBase Reference)
    11. NIST Chemistry Reference: BENZHYDRYLAMINOACETIC ACID, TERT-BUTYL ESTER(158980-46-2)
    12. EPA Substance Registry System: BENZHYDRYLAMINOACETIC ACID, TERT-BUTYL ESTER(158980-46-2)
  • 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: 158980-46-2(Hazardous Substances Data)

158980-46-2 Usage

Uses

Used in Pharmaceutical Industry:
BENZHYDRYLAMINOACETIC ACID, TERT-BUTYL ESTER is used as a synthetic intermediate for the production of 2-Azetidinones, which are crucial in the development of various pharmaceutical compounds. These 2-Azetidinones have potential applications in the treatment of different medical conditions due to their unique chemical structures and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 158980-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,9,8 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 158980-46:
(8*1)+(7*5)+(6*8)+(5*9)+(4*8)+(3*0)+(2*4)+(1*6)=182
182 % 10 = 2
So 158980-46-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H23NO2/c1-19(2,3)22-17(21)14-20-18(15-10-6-4-7-11-15)16-12-8-5-9-13-16/h4-13,18,20H,14H2,1-3H3

158980-46-2SDS

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 Benzhydrylaminoacetic Acid tert-Butyl Ester

1.2 Other means of identification

Product number -
Other names tert-butyl 2-(benzhydrylamino)acetate

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:158980-46-2 SDS

158980-46-2Relevant articles and documents

N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY

-

Page 126, (2010/11/30)

Novel N-hydroxyamide derivatives are disclosed. These N-hydroxyamide derivatives inhibit UPD-3O-(R-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase, an enzyme present in gram negative bacteria and are therefore useful as antimicrobials and antibiotics. Methods of synthesis and of use of the compounds are also disclosed.

A new method of N-benzhydryl deprotection in 2-azetidinone series

Laurent, Mathieu,Belmans, Marc,Kemps, Luc,Ce?re?siat, Marcel,Marchand-Brynaert, Jacqueline

, p. 570 - 576 (2007/10/03)

A mild and efficient procedure for the selective cleavage of N-benzhydryl protecting group of β-lactams is described. The protected 2-azetidinones 4, precursors of carbapenems, were treated with a stoichiometric amount of N-bromosuccinimide and a catalyti

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