4861-85-2 Usage
Description
Isopropyl phenylacetate has a fragrant, rose-like scent and a sweet,
honey-like flavor with a wine undertone.
Chemical Properties
Different sources of media describe the Chemical Properties of 4861-85-2 differently. You can refer to the following data:
1. Isopropyl phenylacetate has a fragrant, rose-like scent; sweet, honey-like flavor with a wine undertone
2. colourless to pale yellow liquid
Taste threshold values
Taste characteristics at 20 ppm: honey, with musty and powdery floral rosy notes.
General Description
Clear pale yellow liquid.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
ISOPROPYL PHENYLACETATE is an ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.
Health Hazard
ACUTE/CHRONIC HAZARDS: ISOPROPYL PHENYLACETATE does not present a serious hazard in normal use. However, it should be borne in mind that the toxicological and physiological properties are not yet well defined.
Fire Hazard
ISOPROPYL PHENYLACETATE is combustible.
Check Digit Verification of cas no
The CAS Registry Mumber 4861-85-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,6 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4861-85:
(6*4)+(5*8)+(4*6)+(3*1)+(2*8)+(1*5)=112
112 % 10 = 2
So 4861-85-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O2/c1-9(2)13-11(12)8-10-6-4-3-5-7-10/h3-7,9H,8H2,1-2H3
4861-85-2Relevant articles and documents
Baldwin,Walker
, p. 3769,3772,3774 (1966)
Photoinduced Diverse Reactivity of Diazo Compounds with Nitrosoarenes
Roy, Sourav,Kumar, Gourav,Chatterjee, Indranil
supporting information, p. 6709 - 6713 (2021/09/08)
A diverse reactivity of diazo compounds with nitrosoarene in an oxygen-transfer process and a formal [2 + 2] cycloaddition is reported. Nitosoarene has been exploited as a mild oxygen source to oxidize an in situ generated carbene intermediate under visible-light irradiation. UV-light-mediated in situ generated ketenes react with nitosoarenes to deliver oxazetidine derivatives. These operationally simple processes exemplify a transition-metal-free and catalyst-free protocol to give structurally diverse α-ketoesters or oxazetidines.
PHOSPHINIC AMIDE PRODRUGS OF TENOFOVIR
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Page/Page column 38, (2020/02/14)
Compounds of Formula I: I and their pharmaceutically acceptable salts are useful for the inhibition of HIV reverse transcriptase. The compounds may also be useful for the prophylaxis or treatment of infection by HIV and in the prophylaxis, delay in the onset or progression, and treatment of AIDS. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antiviral agents, immunomodulators, antibiotics or vaccines.
