N-benzylacetamide

N-benzyl acetamide structural formula

Structural formula

Business number 05ZF
Molecular formula C9H11NO
Molecular weight 149.19
label

N-benzylacetamide,

N-acetyl benzylamine,

N-Benzyl acetamide,

N-acetyl benzylamine,

N-benzylacetamide,

BENZYLACETAMIDE,

N-ACETYLBENZYLAMINE,

N-BENZYLACETAMIDE,

Acetamide, N-benzyl-,

Acetamide,N-(phenylmethyl)-,

Benzylpiperazine-M (benzylamine), AC,

n-(phenylmethyl)-acetamid,

n-(phenylmethyl)acetamide

Numbering system

CAS number:588-46-5

MDL number:MFCD00059204

EINECS number:209-619-2

RTECS number:AB4546300

BRN number:None

PubChem ID:None

Physical property data

1. Physical property data


1. Boiling point 157°C / 2mmHg


2. Melting point (): 61

Toxicological data

None yet

Ecological data

None yet

Molecular structure data

Molecular property data:

1, Molar refractive index:44.05


2, Molar volume (m3/mol):144.6


3, Isotonic specific volume (90.2K):356.6


4, Surface tension (dyne/cm):36.9


5, Polarizability (10-24cm3 ):17.46

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 1

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: 2

6. Topological molecule polar surface area 29.1

7. Number of heavy atoms: 11

8. Surface charge: 0

9. Complexity: 128

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

None yet

Storage method

None yet

Synthesis method

1. Introduction to production methods


Use benzyl chloride to Amination of ammonia water produces benzylamine hydrochloride, which is neutralized with alkali to obtain benzylamine, which is then acylated with acetic acid to obtain this product.

Purpose

2. Purpose


Sulfamirone vinegar Intermediates of acid salts.

This article is from the Internet, does not represent the position of Toluene diisocyanate reproduced please specify the source.https://www.chemicalchem.com/archives/30079

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