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Merck
CN

277037

Sigma-Aldrich

(1R,2R)-(+)-1-Phenylpropylene oxide

97%

Synonym(s):

(2R,3R)-(+)-2-Methyl-3-phenyloxirane

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About This Item

Empirical Formula (Hill Notation):
C9H10O
CAS Number:
Molecular Weight:
134.18
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22
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Assay

97%

form

liquid

optical activity

[α]20/D +110°, neat

optical purity

ee: 99% (GLC)

refractive index

n20/D 1.518 (lit.)

bp

201-207 °C (lit.)

density

1.006 g/mL at 25 °C (lit.)

SMILES string

C[C@H]1O[C@@H]1c2ccccc2

InChI

1S/C9H10O/c1-7-9(10-7)8-5-3-2-4-6-8/h2-7,9H,1H3/t7-,9+/m1/s1

InChI key

YVCOJTATJWDGEU-APPZFPTMSA-N

Application

Chiral building block. Tool for studying enzyme hydrolysis rates.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

156.2 °F - closed cup

Flash Point(C)

69 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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B D Hammock et al.
Biochemical pharmacology, 32(7), 1155-1164 (1983-04-01)
The initial rates of hydration of sixteen epoxides in the presence of cytosolic and microsomal fractions of mouse liver were determined. 1,2-Disubstituted trans-epoxides were found to be excellent, selective substrates for the cytosolic epoxide hydrolase, while 1,2-cis-epoxides were poorly hydrated

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