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Key Documents

140856

Sigma-Aldrich

3-苯基-1-丙醇

98%

同義詞:

3-苯丙醇, 氢化肉桂醇

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About This Item

線性公式:
C6H5(CH2)3OH
CAS號碼:
分子量::
136.19
Beilstein:
1857542
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

98%

形狀

liquid

折射率

n20/D 1.526 (lit.)

bp

119-121 °C/12 mmHg (lit.)

mp

−18 °C (lit.)

密度

1.001 g/mL at 20 °C (lit.)

官能基

hydroxyl

SMILES 字串

OCCCc1ccccc1

InChI

1S/C9H12O/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6,10H,4,7-8H2

InChI 密鑰

VAJVDSVGBWFCLW-UHFFFAOYSA-N

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一般說明

3-苯基-1-丙醇是一种香味成分

應用

3-苯基-1-丙醇被用于使用水溶性有机金属配合物研究 反式 -肉桂醛的氢化反应。在 (S)-和 (R)-达泊西汀的对映选择性合成中用作起始试剂

象形圖

Corrosion

訊號詞

Danger

危險聲明

危險分類

Eye Dam. 1 - Skin Corr. 1B

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

248.0 °F - closed cup

閃點(°C)

120 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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The regioselective biphasic hydrogenation of trans-cinnaldehyde by meta sulfonatophenyl-diphenylphosphine (TPPMS) Ru (II) and Os (II) species. The influence of ionic strength, ligand tensoactivity and metal nature in the selective production of the unsaturated alcohol.
Lopez-Linares F, et al.
J. Mol. Catal. A: Chem., 145(1), 61-68 (1999)
D Belsito et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 49 Suppl 2, S256-S267 (2011-08-09)
The cinnamyl phenylpropyl fragrance ingredients are a diverse group of chemical structures that have similar metabolic and toxicity profiles. A toxicological and dermatological review of these fragrance ingredients is presented. The common characteristic structural element of cinnamyl phenylpropyl materials is
Jörgen Samuelsson et al.
Journal of chromatography. A, 1217(46), 7215-7221 (2010-10-12)
The elution by characteristic points (ECP) method is a very rapid and precise method for determination of the phase system equilibrium of phase systems in broad solute concentration ranges. Thus, the method is especially suitable for rapid characterization of high
Soyeong Kang et al.
The Journal of organic chemistry, 75(1), 237-240 (2009-12-05)
A highly efficient, enantioselective sequence has been developed for the synthesis of (S)- and (R)-dapoxetine. The pathways involve the intermediacy of the 6-membered-ring sulfamate esters 4, which were generated by Du Bois asymmetric C-H amination reactions of the prochiral sulfamate
S P Bhatia et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 49 Suppl 2, S246-S251 (2011-08-23)
A toxicologic and dermatologic review of 3-phenyl-1-propanol when used as a fragrance ingredient is presented. 3-Phenyl-1-propanol is a member of the fragrance structural group cinnamyl phenylpropyl compounds. The common characteristic structural element of cinnamyl phenylpropyl materials is an aryl substituted

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