88753-46-2 Usage
Chemical composition
The compound is composed of 1,3-butanediol, phenylmethoxy, acetate, and benzoate groups.
Physical state
It is a stable, colorless liquid.
Solvent
It is commonly used as a solvent in the formulation of pharmaceuticals, cosmetics, and personal care products.
Viscosity agent
It can be used as a viscosity agent in various formulations.
Moisturizer
It has moisturizing properties and can be used in personal care products.
Flavoring agent
It can be utilized as a flavoring agent in food and beverages.
Versatile properties
The chemical has potential applications in various industries due to its versatile properties.
Wide range of consumer products
It can be found in a wide range of consumer products, including pharmaceuticals, cosmetics, personal care products, and the food and beverage industry.
Check Digit Verification of cas no
The CAS Registry Mumber 88753-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,5 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88753-46:
(7*8)+(6*8)+(5*7)+(4*5)+(3*3)+(2*4)+(1*6)=182
182 % 10 = 2
So 88753-46-2 is a valid CAS Registry Number.
88753-46-2Relevant academic research and scientific papers
NUCLEOPHILIC DISPLACEMENT REACTIONS OF THE METHANESULFONATES OF THE 1-O-BENZOYL-1,2-, -1,3-, AND -1,4-GLYCOLS
Takano, Seiichi,Hirama, Michiyasu,Seya, Kazuhiko,Ogasawara, Kunio
, p. 4233 - 4236 (2007/10/02)
Nucleophilic displacement reactions of the methanesulfonates (8a-c) of the 1-O-benzoyl-1,2-, -1,3-, and -1,4-glycols (7a-c) with potassium acetate in boiling acetic anhydride have been examined.Both benzoyloxy-group participation pathway (path A) and SN2 displacement pathway (path B) have been involved in the 1,2-(8a)- and 1,3-(8b)-substrates to give a mixture of the primary (10a,b) and the secondary (11a,b) acetates with complete inversion of chiralities.On the other hand, only SN2 displacement pathway (path B) has been involved in the 1,4-substrate (8c) to give the secondary acetate (11c) with inversion of the chirality.
