2-METHYL-3-PHENYL-2-PROPEN-1-OL CAS#: 1504-55-8

2-METHYL-3-PHENYL-2-PROPEN-1-OL Basic information

Product Name:

2-METHYL-3-PHENYL-2-PROPEN-1-OL

Synonyms:

trans-2-Methyl-3-phenyl-2-propen-1-ol 95%
2-methyl-3-phenyl-2-propen-1-o
(E)-2-Methyl-3-phenylprop-2-en-1-ol
2-Methyl-3-phenylprop-2-en-1-ol
(E)-2-methyl-3-phenyl-2-propen-1-ol
3-phenyl-2-methyl-propen-2-ol-1
alpha-methyl-cinnamylalcoho
methylcinnamicalcohol

CAS:

1504-55-8

MF:

C10H12O

MW:

148.2

EINECS:

216-128-7

Product Categories:

Acyclic
Alkenes
Organic Building Blocks

Mol File:

1504-55-8.mol

More

Less

2-METHYL-3-PHENYL-2-PROPEN-1-OL Chemical Properties

Melting point:: 24-25 °C(Solv: ligroine (8032-32-4))
Boiling point:: 77 °C0.1 mm Hg(lit.)
Density: 1.03 g/mL at 25 °C(lit.)
refractive index: n20/D 1.572(lit.)
Flash point:: >230 °F
solubility: Almost insoluble in water, soluble in alcohol and oils.?
pka: 14?+-.0.10(Predicted)
form: powder to lump to clear liquid
color: White or Colorless to Light yellow
Odor: at 100.00 %. sweet balsam floral oriental styrax
Odor Type: balsamic
LogP: 1.929 (est)
EPA Substance Registry System: 2-Propen-1-ol, 2-methyl-3-phenyl- (1504-55-8)

More

Less

Safety Information

Hazard Codes: Xi
Risk Statements: 36/37/38
Safety Statements: 26-37/39
WGK Germany: 2
RTECS: GE2340000
HS Code: 2906290090
Toxicity: The acute oral LD₅₀ in rats was reported as 2.4 ml/kg (1.9-3.0 ml/kg) (Levenstein, 1974). The acute dermal LD₅₀ in rabbits exceeded 5 g/kg (Levenstein, 1974).

MSDS

Language:English Provider:SigmaAldrich

More

Less

2-METHYL-3-PHENYL-2-PROPEN-1-OL Usage And Synthesis

Occurrence

Has apparently not been reported to occur in nature

Uses

trans-2-Methyl-3-phenyl-2-propen-1-ol was used in the preparation of 5-methyl-4-phenyl-5-hexen-2-one.

Preparation

By selective hydrogenation of methylcinnamic aldehyde

Synthesis Reference(s)

Journal of the American Chemical Society, 117, p. 10417, 1995 DOI: 10.1021/ja00146a041

Metabolism

Cinnamic alcohol is mainly metabolized to benzoic acid, presumably via cinnamic acid, but substitution apparently prevents oxidation to benzoic acid, since 2-ethylcinnamic alcohol ( C 6H 5CH:C(C 2H 5)CH 2O H ) is partly (30-33%) excreted as α-ethylcinnamic acid (Williams, 1959)

2-METHYL-3-PHENYL-2-PROPEN-1-OLSupplier

J & K SCIENTIFIC LTD.

Tel: 010-82848833 400-666-7788
Email: jkinfo@jkchemical.com

TCI (Shanghai) Development Co., Ltd.

Tel: 021-67121386
Email: Sales-CN@TCIchemicals.com

Energy Chemical

Tel: 021-021-58432009 400-005-6266
Email: sales8178@energy-chemical.com

Adamas Reagent, Ltd.

Tel: 400-6009262 16621234537
Email: chenyj@titansci.com

Syntechem Co.,Ltd

Tel
Email: info@syntechem.com

More

Less