7492-67-3 Usage
Description
FEMA 2310, also known as Citronellyl oxyacetaldehyde, is a synthetic organic compound with a strong, floral odor. It is characterized by a citrus, bitter, and floral taste with a slight soapy and woody nuance at a concentration of 20 ppm. However, it has not been reported to occur naturally.
Uses
Used in Flavor Industry:
FEMA 2310 is used as a flavoring agent for its citrus, bitter, and floral taste characteristics. It is commonly used in the formulation of food and beverages to impart a pleasant and refreshing flavor.
Used in Fragrance Industry:
FEMA 2310 is used as a fragrance ingredient for its strong, floral odor. It is widely used in the production of perfumes, colognes, and other scented products to provide a long-lasting and pleasant scent.
Used in Cosmetic Industry:
FEMA 2310 is used as a scent enhancer in various cosmetic products such as soaps, shampoos, and lotions. Its floral and citrus notes add a refreshing and uplifting effect to these products, making them more appealing to consumers.
Used in Aromatherapy:
FEMA 2310 can be used in aromatherapy for its calming and uplifting properties. Its floral and citrus scent can help create a relaxing and soothing atmosphere, promoting mental well-being and stress relief.
Preparation
Interaction of bromoacetals with sodium or potassium alcoholates.
Check Digit Verification of cas no
The CAS Registry Mumber 7492-67-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7492-67:
(6*7)+(5*4)+(4*9)+(3*2)+(2*6)+(1*7)=123
123 % 10 = 3
So 7492-67-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O2/c1-11(2)5-4-6-12(3)7-9-14-10-8-13/h5,8,12H,4,6-7,9-10H2,1-3H3
7492-67-3Relevant articles and documents
Cyclopropenation of alkylidene carbenes derived from α-silyl ketones
Li, Jingwei,Sun, Chunrui,Lee, Daesung
supporting information; experimental part, p. 6640 - 6641 (2010/07/04)
A new cyclopropanation reaction involving Cα-Si bond insertion of alkylidene carbenes derived from α-silyl ketones has been developed. This unprecedented alkylidene carbene reactivity features excellent selectivity for insertion into Cα-Si bonds rather than insertion into Cγ-H bonds or addition to,δ-double or -triple bonds. The selectivity trend clearly indicates that the α-oxygen in the tether significantly promotes Cγ-H insertion, although the Cα-Si bond insertion still competes effectively.
Process for preparing substituted oxyacetaldehydes and acetals thereof
-
, (2008/06/13)
A process is described for the preparation of substituted oxyacetaldehydes and acetals thereof according to the reaction sequence: STR1 WHEREIN R1 and R2 are each lower alkyl or R1 and R2, taken together form a lower alkylene group; wherein R3 is alkyl, alkenyl or alkadienyl and X is halogen selected from the group consisting of chlorine and bromine, the reaction (i) being carried out (1) using a "phase transfer agent" and (2) in a two phase system.