6270-03-7

Basic information

• Product Name: PHENETHYL ALCOHOL, BETA-HYDROXY:DIACETATE
• Synonyms: PHENETHYL ALCOHOL, BETA-HYDROXY:DIACETATE;PHENYL GLYCOL DIACETATE;1,2-Ethanediol,1-phenyl-,diacetate;2-ethanediol,1-phenyl-diacetate;phenylethylenedi(acetate);phenylethane-1,2-diol diacetate;1-Phenyl-1,2-diacetoxyethane;1-Phenyl-1,2-ethanediol diacetate
• CAS NO: 6270-03-7
• Molecular Formula: C₁₂H₁₄O₄
• Molecular Weight: 222.24
• EINECS: 228-445-8
• Mol File: 6270-03-7.mol
• Article Data: 94

Chemical Properties

• Appearance: /
• CAS DataBase Reference: PHENETHYL ALCOHOL, BETA-HYDROXY:DIACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: PHENETHYL ALCOHOL, BETA-HYDROXY:DIACETATE(6270-03-7)
• EPA Substance Registry System: PHENETHYL ALCOHOL, BETA-HYDROXY:DIACETATE(6270-03-7)

Safety Data

• Hazardous Substances Data: 6270-03-7(Hazardous Substances Data)

Usage

Uses

Used in Perfume Industry:
PHENETHYL ALCOHOL, BETA-HYDROXY:DIACETATE is used as a fragrance ingredient for its pleasant floral scent, enhancing the overall scent profile of perfumes and making them more appealing to consumers.
Used in Skincare Products:
PHENETHYL ALCOHOL, BETA-HYDROXY:DIACETATE is used as a key ingredient in skincare products for its pleasant floral scent and its ability to improve the stability and longevity of the fragrance in these products.
Used in Personal Care Products:
PHENETHYL ALCOHOL, BETA-HYDROXY:DIACETATE is used as a fragrance ingredient in personal care products, such as soaps, shampoos, and body lotions, to provide a pleasant floral scent and improve the stability and longevity of the fragrance.
Used in Cosmetic Products:
PHENETHYL ALCOHOL, BETA-HYDROXY:DIACETATE is used as a fragrance ingredient in cosmetic products, such as lipsticks, foundations, and eyeshadows, to provide a pleasant floral scent and improve the stability and longevity of the fragrance.
Used in Antimicrobial Applications:
PHENETHYL ALCOHOL, BETA-HYDROXY:DIACETATE is used as a preservative in products that require protection against bacteria and fungi due to its antimicrobial properties, ensuring the safety and longevity of the products.

InChI:InChI=1/C8H8.2C2H4O2/c1-2-8-6-4-3-5-7-8;2*1-2(3)4/h2-7H,1H2;2*1H3,(H,3,4)/p-2

Upstream product

• 93-56-1 phenylethane 1,2-diol 
• 108-24-7 acetic anhydride 
• 100-42-5 styrene 
• 546-67-8 lead(IV) tetraacetate 
• 108-05-4 vinyl acetate 
• 107866-54-6 1-acetyl-1H-1,2,3-triazolo<4,5-b>pyridine 
• 75178-12-0 2,2'-bipyridyl-6-yl acetate 
• 75-36-5 acetyl chloride 
• 82240-84-4 2-Chloro-4-phenyl-1,3,2-dioxastibole 
• 82240-85-5 2-Chloro-4-phenyl-1,3,2-dioxarsole 
• 18735-16-5 α,β-diacetoxy-styrene 
• 71-43-2 benzene 
• 96-09-3 styrene oxide 
• 100-52-7 benzaldehyde 

Downstream Products

• 127707-63-5 2-phenyl-2-hydroxyethyl acetate 
• 16355-00-3 (R)-1-phenyl-1,2-ethanediol 
• 25779-13-9 (S)-1-phenyl-1,2-ethanediol 
• 104-62-1 formic acid phenethyl ester 
• 100-41-4 ethylbenzene 
• 103-45-7 acetic acid phenethyl ester 
• 258523-87-4 (R)-1-acetoxy-1-phenylethanol 
• 10522-02-8 (S)-1-acetoxy-1-phenylethanol 

Relevant articles and documents

Tandem Acid/Pd-Catalyzed Reductive Rearrangement of Glycol Derivatives

Herein, we describe the acid/Pd-tandem-catalyzed transformation of glycol derivatives into terminal formic esters. Mechanistic investigations show that the substrate undergoes rearrangement to an aldehyde under [1,2] hydrogen migration and cleavage of an oxygen-based leaving group. The leaving group is trapped as its formic ester, and the aldehyde is reduced and subsequently esterified to a formate. Whereas the rearrangement to the aldehyde is catalyzed by sulfonic acids, the reduction step requires a unique catalyst system comprising a PdII or Pd0 precursor in loadings as low as 0.75 mol % and α,α′-bis(di-tert-butylphosphino)-o-xylene as ligand. The reduction step makes use of formic acid as an easy-to-handle transfer reductant. The substrate scope of the transformation encompasses both aromatic and aliphatic substrates and a variety of leaving groups.

PREPARATION OF DIESTERS OF (METH)ACRYLIC ACID FROM EPOXIDES

The application relates to a process for preparing a (meth)acrylic acid diester by reacting a (meth)acrylic acid anhydride with an epoxide in the presence of a catalyst system comprising a first and/or second catalyst in combination with a co-catalyst. The first catalyst is a halide of Mg or a trifluoromethanesulfonate of a rare earth element; the second catalyst is a Cr(lll) salt; and the co- catalyst is a tertiary amine, a quaternary ammonium salt, a tertiary phosphine or a quaternary phosphonium salt.

SYNTHESIS OF HYPERVALENT IODINE REAGENTS WITH DIOXYGEN

Methods of synthesis of hypervalent iodine reagents and methods for oxidation of organic compounds are disclosed.