2-Methyl-3-phenyl-2-propen-1-ol

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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-phenyl-2-propen-1-ol;3-phenyl-2-methyl-propen-2-ol-1;alpha-methyl-cinnamylalcoho;methylcinnamicalcohol;TRANS-2-METHYL-3-PHENYL-2-PROPEN-1-OL;ALPHA-METHYLCINNAMYL ALCOHOL
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
2-Methyl-3-phenyl-2-propen-1-ol Structure
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.)
Fp >230 °F
solubility Almost insoluble in water, soluble in alcohol and oils.
pka14+-.0.10(Predicted)
form powder to lump to clear liquid
color White or Colorless to Light yellow
Odorat 100.00 %. sweet balsam floral oriental styrax
Odor Typebalsamic
Cosmetics Ingredients FunctionsPERFUMING
InChI1S/C10H12O/c1-9(8-11)7-10-5-3-2-4-6-10/h2-7,11H,8H2,1H3/b9-7+
InChIKeyLLNAMUJRIZIXHF-VQHVLOKHSA-N
SMILES[H]\C(=C(\C)CO)c1ccccc1
LogP1.929 (est)
EPA Substance Registry System2-Propen-1-ol, 2-methyl-3-phenyl- (1504-55-8)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39
WGK Germany 2
RTECS GE2340000
TSCA TSCA listed
HS Code 2906290090
Storage Class10 - Combustible liquids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
toxicityThe 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 Information
ProviderLanguage
SigmaAldrich English
2-Methyl-3-phenyl-2-propen-1-ol Usage And Synthesis
OccurrenceHas apparently not been reported to occur in nature
Usestrans-2-Methyl-3-phenyl-2-propen-1-ol was used in the preparation of 5-methyl-4-phenyl-5-hexen-2-one.
PreparationBy selective hydrogenation of methylcinnamic aldehyde
Synthesis Reference(s)Journal of the American Chemical Society, 117, p. 10417, 1995 DOI: 10.1021/ja00146a041
MetabolismCinnamic 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-ol Preparation Products And Raw materials
Tag:2-Methyl-3-phenyl-2-propen-1-ol(1504-55-8) Related Product Information
EOSIN B AFLATOXIN G1 Solvent Red 43 Phenylfluorone Sulforhodamine B alpha-Phenylcinnamic acid Coumarin-3-carboxylic acid alpha-Methylcinnamic acid Rhodamine 6g tetrafluoroborate Ethyl eosin 2-Methyl-1-phenylpropene Diethyl benzylidenemalonate alpha-Cyanocinnamic acid ethyl ester 2-Methyl-3-phenyl-2-propen-1-ol alpha-Cyano-4-hydroxycinnamic acid 2,3-Diphenylmaleic anhydride 2-Methyl-1-phenyl-2-propen-1-ol alpha-Cyano-3-hydroxycinnamic acid