(S)-(+)-Mandelamide

Base Information

Chemical Name:(S)-(+)-Mandelamide
CAS No.:24008-63-7
Molecular Formula:C8H9 N O2
Molecular Weight:151.165
Hs Code.:2924299090
UNII:DD3HYR9MHB
DSSTox Substance ID:DTXSID10356025
Nikkaji Number:J74.045D
Wikidata:Q82135150
Mol file:24008-63-7.mol

Synonyms:(S)-(+)-Mandelamide;24008-63-7;(S)-2-Hydroxy-2-phenylacetamide;(2S)-2-hydroxy-2-phenylacetamide;(s)-mandelamide;(S)-Mandeloamide;L-(+)-Mandelamide;Mandelamide, (S)-;Mandelamide, (+)-;DD3HYR9MHB;(S)-(+)-Mandelic acid amide;(S)-(+)-2-Hydroxy-2-phenylacetamide;(s)-mandelamid;(S)-mandelic amide;UNII-DD3HYR9MHB;(S)-mandelic acid amide;SCHEMBL4026125;DTXSID10356025;CHEBI:134268;(S)-(+)-Mandelamide >=97%;ZAA00863;(S)-(+)-Mandelamide, >=97%;MFCD08704381;(alphaS)-alpha-Hydroxybenzeneacetamide;AKOS016015890;BENZENEACETAMIDE, A-HYDROXY-,(AS)-;Benzeneacetamide, alpha-hydroxy-, (alphaS)-;E85993;(.ALPHA.S)-.ALPHA.-HYDROXYBENZENEACETAMIDE;J-015311;BENZENEACETAMIDE, .ALPHA.-HYDROXY-, (.ALPHA.S)-

Suppliers and Price of (S)-(+)-Mandelamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
(S)-Mandelamide
5 g
$ 195.00

TRC
(S)-Mandelamide
1 g
$ 60.00

Sigma-Aldrich
(S)-(+)-Mandelamide ≥97%
1g
$ 52.40

Sigma-Aldrich
(S)-(+)-Mandelamide ≥97%
5g
$ 197.00

Crysdot
(S)-2-Hydroxy-2-phenylacetamide 95+%
5g
$ 372.00

Crysdot
(S)-2-Hydroxy-2-phenylacetamide 95+%
10g
$ 512.00

American Custom Chemicals Corporation
(S)-(+)-MANDELAMIDE 95.00%
1G
$ 659.01

Alichem
(S)-2-Hydroxy-2-phenylacetamide
25g
$ 1299.87

Alichem
(S)-2-Hydroxy-2-phenylacetamide
10g
$ 744.37

Alichem
(S)-2-Hydroxy-2-phenylacetamide
5g
$ 552.08

Total 11 raw suppliers

Chemical Property of (S)-(+)-Mandelamide

Chemical Property:

Vapor Pressure:2.33E-05mmHg at 25°C
Boiling Point:345.5°C at 760 mmHg
Flash Point:162.7°C
PSA：63.32000
Density:1.246g/cm³
LogP:0.90560
XLogP3:0
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:151.063328530
Heavy Atom Count:11
Complexity:141

Purity/Quality:

98%,99%, ^*data from raw suppliers

(S)-Mandelamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(C(=O)N)O
Isomeric SMILES:C1=CC=C(C=C1)[C@@H](C(=O)N)O
Uses Produced by the conversion of (S)-mandelonitrile by the arylacetonitrilase of Pseudomonas fluorescens EBC191

Technology Process of (S)-(+)-Mandelamide

There total 97 articles about (S)-(+)-Mandelamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 69.0%

: 724-92-5
N-cicloesil-α-ossofenilacetamide

: 4410-31-5,24008-62-6,24008-63-7,4358-86-5
(RS)-mandelamide

: 108-94-1,11119-77-0,9003-41-2,9075-99-4
cyclohexanone

Guidance literature:: With sulfuric acid; In ethanol; water; Product distribution; Mechanism; Irradiation; other solvents;
DOI:10.1039/P19810001357

Reference yield: 46.0%

: 611-71-2,611-72-3,17199-29-0,90-64-2
MANDELIC ACID

: 17199-29-0
(S)-Mandelic acid

: 4358-86-5,4410-31-5,24008-63-7,24008-62-6
(2R)-mandelamide

: 611-71-2
(R)-Mandelic Acid

Guidance literature:: With ammonium bicarbonate; In water; dimethyl sulfoxide; at 50 ℃; for 8h; Time; Reagent/catalyst; Temperature; Enzymatic reaction;
DOI:10.3109/10242422.2014.971120