CAS 4393-06-0

(1R)-1-phenylprop-2-en-1-ol

Description:

(1R)-1-phenylprop-2-en-1-ol, also known as (R)-phenylpropenol, is an organic compound characterized by its structure, which features a phenyl group attached to a propene chain with a hydroxyl (-OH) functional group. This compound is a chiral molecule, meaning it has non-superimposable mirror images, with the (1R) configuration indicating the specific spatial arrangement of its atoms. It typically appears as a colorless to pale yellow liquid and has a pleasant, floral odor, making it of interest in the fragrance industry. The compound is soluble in organic solvents and has limited solubility in water due to its hydrophobic phenyl group. Its reactivity includes participation in various organic reactions, such as oxidation and esterification, and it can serve as a precursor in the synthesis of more complex molecules. Additionally, (1R)-1-phenylprop-2-en-1-ol may exhibit biological activity, which could be relevant for applications in pharmaceuticals or agrochemicals. Safety data should be consulted for handling and exposure guidelines.

Formula: C₉H₁₀O

InChI: InChI=1/C9H10O/c1-2-9(10)8-6-4-3-5-7-8/h2-7,9-10H,1H2/t9-/m1/s1

SMILES: C=C[C@H](c1ccccc1)O

3-Phenylpropene-3-ol

CAS: 4393-06-0

Formula: C₉H₁₀O

Purity: 98%

Color and Shape: Liquid

Molecular weight: 134.1751

Ref: IN-DA00DK19

1-Phenylprop-2-En-1-Ol

CAS: 4393-06-0

1-Phenylprop-2-En-1-Ol

Purity: 98%

Molecular weight: 134.18g/mol

Ref: 54-OR1027753

1-phenylprop-2-en-1-ol

CAS: 4393-06-0

1-phenylprop-2-en-1-ol

Purity: ≥95%

Molecular weight: 134.18g/mol

Ref: 54-BUP10421

1-phenylprop-2-en-1-ol

CAS: 4393-06-0

1-phenylprop-2-en-1-ol, used in polymer synthesis, has antifungal and anti-inflammatory properties.

Formula: C₉H₁₀O

Purity: 95.00%

Color and Shape: Solid

Molecular weight: 134.18

Ref: TM-T50007

1-Phenylprop-2-en-1-ol

CAS: 4393-06-0

Formula: C₉H₁₀O

Purity: 98% (stabilized with TBC)

Color and Shape: Liquid

Molecular weight: 134.178

Ref: 10-F438205

α-Vinylbenzyl alcohol

CAS: 4393-06-0

α-Vinylbenzyl alcohol is a chiral compound with a hydroxyl group. It is an allylation product of hydrochloric acid and allyl chloride. α-Vinylbenzyl alcohol has been shown to be effective against allergic reactions in human serum, which are caused by the release of histamine. This chemical compound also has nucleophilic attack capabilities that can produce reaction products such as malonic acid or allyl carbonate. The effective dose for this drug is not known, but it may be around 1mg/kg of body weight.

Formula: C₉H₁₀O

Purity: Min. 95%

Molecular weight: 134.17 g/mol

Ref: 3D-EAA39306