16939-73-4 Usage
Description
ACETIC ACID TRANS-2-HEPTEN-1-YL ESTER is a colorless liquid with a fresh leaf aroma. It has a medium strength odor and is classified as a fruity type. It is recommended to smell it in a 10.00% solution or less.
Uses
Used in Flavor and Fragrance Industry:
ACETIC ACID TRANS-2-HEPTEN-1-YL ESTER is used as a flavoring agent for its fresh leaf aroma and fruity scent. It adds a unique and pleasant aroma to various food and beverage products.
Used in Perfumery:
ACETIC ACID TRANS-2-HEPTEN-1-YL ESTER is used as a fragrance ingredient in perfumes and colognes. Its fresh and fruity scent adds a refreshing and natural touch to the overall fragrance profile.
Used in Cosmetics and Personal Care Products:
ACETIC ACID TRANS-2-HEPTEN-1-YL ESTER is used in cosmetics and personal care products to provide a pleasant and refreshing scent. It can be used in products such as lotions, creams, shampoos, and soaps to enhance the sensory experience for the user.
Used in Aromatherapy:
ACETIC ACID TRANS-2-HEPTEN-1-YL ESTER can be used in aromatherapy for its fresh and uplifting scent. It may help to create a calming and relaxing atmosphere, promoting a sense of well-being and reducing stress.
Check Digit Verification of cas no
The CAS Registry Mumber 16939-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,9,3 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16939-73:
(7*1)+(6*6)+(5*9)+(4*3)+(3*9)+(2*7)+(1*3)=144
144 % 10 = 4
So 16939-73-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O2/c1-3-4-5-6-7-8-11-9(2)10/h6-7H,3-5,8H2,1-2H3/b7-6+
16939-73-4Relevant articles and documents
Stereoselective Preparation of (E)-Allyl Alcohols via Radical Elimination from anti-γ-Phenylthio-β-nitro Alcohols
Kamimura, Akio,Ono, Noboru
, p. 1278 - 1280 (1988)
Phenylthio and hydroxymethyl groups may be introduced into nitroalkenes stereoselectively by treatment with benzenethiol and aqueous formaldehyde to give anti-γ-phenylthio-β-nitro alcohols, which are converted into (E)-allyl alcohols via radical elimination induced by Bu3SnH.
