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87708-44-9

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87708-44-9 Usage

Molecular Weight

222.29 g/mol

Appearance

Colorless to pale yellow liquid

Aroma

Sweet, fruity, and floral

Usage

Flavoring agent in the food and beverage industry (fruit-flavored products, confectionery, baked goods) and fragrance industry (perfumes, colognes, personal care products)

Properties

Strong and long-lasting aroma

Safety

Considered safe for consumption and use in cosmetics when used in accordance with regulatory guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 87708-44-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,0 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87708-44:
(7*8)+(6*7)+(5*7)+(4*0)+(3*8)+(2*4)+(1*4)=169
169 % 10 = 9
So 87708-44-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H18O2/c1-4-10(2)13(14)15-11(3)12-8-6-5-7-9-12/h5-11H,4H2,1-3H3

87708-44-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenylethyl 2-methylbutanoate

1.2 Other means of identification

Product number -
Other names 1-Phenylethyl 2-methylbutyrate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:87708-44-9 SDS

87708-44-9Downstream Products

87708-44-9Relevant articles and documents

Highly enantioselective iridium-catalyzed hydrogenation of α,β-unsaturated esters

Li, Jia-Qi,Quan, Xu,Andersson, Pher G.

, p. 10609 - 10616 (2012/11/07)

α,β-Unsaturated esters have been employed as substrates in iridium-catalyzed asymmetric hydrogenation. Full conversions and good to excellent enantioselectivities (up to 99 % ee) were obtained for a broad range of substrates with both aromatic- and aliphatic substituents on the prochiral carbon. The hydrogenated products are highly useful as building blocks in the synthesis of a variety of natural products and pharmaceuticals. Asymmetric hydrogenation: A variety of α,β-unsaturated esters were hydrogenated with high enantioselectivities (see scheme). The hydrogenated products have been used in synthetic transformations as well as in formal total syntheses. Copyright

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