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Merck
CN

51432

(S)-(−)-α-Ethylbenzylamine

≥95.0% (GC)

Synonym(s):

(S)-(−)-1-Phenylpropylamine

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About This Item

Empirical Formula (Hill Notation):
C9H13N
CAS Number:
Molecular Weight:
135.21
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2412016
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Product Name

(S)-(−)-α-Ethylbenzylamine, ≥95.0% (GC)

InChI

1S/C9H13N/c1-2-9(10)8-6-4-3-5-7-8/h3-7,9H,2,10H2,1H3/t9-/m0/s1

SMILES string

CC[C@H](N)c1ccccc1

InChI key

AQFLVLHRZFLDDV-VIFPVBQESA-N

assay

≥95.0% (GC)

optical activity

[α]20/D −20±2°, neat

optical purity

enantiomeric ratio: ≥99.0:1.0 (GC)

refractive index

n20/D 1.520

density

0.940 g/mL at 20 °C (lit.)

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Application

(S)-(−)-α-Ethylbenzylamine can be used:
  • To prepare optically active copolyacrylate polymers with sensing and chiroptical properties.
  • As a chiral auxiliary in the preparation of enantioenriched indanone derived α-SCF2H β-keto esters.

pictograms

CorrosionExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

170.6 °F

flash_point_c

77 °C

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Asymmetric Electrophilic Difluoromethylthiolation of Indanone-Based β-Keto Esters Using Difluoromethanesulfonyl Hypervalent Iodonium Ylides
Gondo S, et al.
Molecules (Basel), 24(2), 221-221 (2019)
Synthesis and characterization of new optically active poly (acrylamide/methacrylurea-co-vinyl acetate) copolymers with dansyl units
Murariu M and Buruiana EC
Designed Monomers and Polymers, 18(2), 118-128 (2015)

Articles

Chiral amines have found widespread application in asymmetric synthesis serving, for instance, as chiral bases in enantioselective deprotonation reactions or being valuable substances for resolving racemic mixtures of acids.

手性胺已广泛用于不对称合成,例如用作对映选择性去质子化反应中的手性碱,或用于拆分消旋的酸。

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