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33545-23-2

MEA-BENZOATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 33545-23-2 Structure

  • Basic information

    1. Product Name: MEA-BENZOATE
    2. Synonyms: MEA-BENZOATE;2-Aminoethanol benzoate (ester);2-Aminoethyl benzoate;Ethanol, 2-amino-, benzoate (ester)
    3. CAS NO:33545-23-2
    4. Molecular Formula: C9H11NO2
    5. Molecular Weight: 165.18914
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 33545-23-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 271.8°Cat760mmHg
    3. Flash Point: 132.4°C
    4. Appearance: /
    5. Density: 1.119g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: MEA-BENZOATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: MEA-BENZOATE(33545-23-2)
    11. EPA Substance Registry System: MEA-BENZOATE(33545-23-2)

  • 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: 33545-23-2(Hazardous Substances Data)

33545-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33545-23-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,5,4 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 33545-23:
(7*3)+(6*3)+(5*5)+(4*4)+(3*5)+(2*2)+(1*3)=102
102 % 10 = 2
So 33545-23-2 is a valid CAS Registry Number.

33545-23-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-aminoethyl benzoate

1.2 Other means of identification

Product number -
Other names 1-Amino-2-benzoyloxy-aethan

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:33545-23-2 SDS

33545-23-2Relevant articles and documents

Imidazole-catalyzed monoacylation of symmetrical diamines

Verma, Sanjeev K.,Acharya,Kaushik

body text, p. 4232 - 4235 (2010/11/04)

Figure Presented. An imidazole-catalyzed protocol for monoacylation of symmetrical diamines has been developed. The protocol gave selective monoacylation of aliphatic (cyclic and acyclic) primary and secondary diamines. In the reaction, imidazole acts as both catalyst and a leaving group. Different monoacylated piperazines and other diamines were synthesized at room temperature in an ethanol/water solvent system.

N-heterocyclic carbene-catalyzed amidation of unactivated esters with amino alcohols

Movassaghi, Mohammad,Schmidt, Michael A.

, p. 2453 - 2456 (2007/10/03)

(Chemical Equation Presented) A catalytic amidation of unactivated esters with amino alcohols is described. A series of solution studies in addition to the first X-ray structure of a carbene-alcohol complex support a carbene-base nucleophile activation mechanism.

Al2O3/MeSO3H (AMA) as a new reagent with high selective ability for monoesterification of diols

Sharghi, Hashem,Sarvari, Mona Hosseini

, p. 3627 - 3633 (2007/10/03)

A new facile method for monoesterification of diols has been developed. A variety of diols, in particular oligoethylene glycols, were selectively monoesterified in excellent yields by reaction with aromatic and aliphatic acids in the presence of Al2O3/MeSO3H as a new reagent without use of any solvents.

Highly selective methodology for the direct conversion of aromatic aldehydes to glycol monoesters

Sharghi, Hashem,Sarvari, Mona Hosseini

, p. 4096 - 4099 (2007/10/03)

Al2O3/MeSO3H (AMA) was found to be an extremely efficient reagent for the conversion of aromatic aldehydes and diols to glycol monoesters. The remarkable selectivity achieved with this reagent is an attractive feature of t

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