7501-94-2 Usage
Type of alcohol
Secondary alcohol
Hydroxyl group attachment
To a carbon atom bonded to two other carbon atoms
Chemical structure
Butane backbone with a hydroxyl group on the second carbon atom, and two phenyl groups on the first and third carbon atoms
Applications
a. Organic synthesis as a chiral auxiliary
b. Building block for pharmaceuticals and fine chemicals
c. Fragrance ingredient in perfumes
d. Flavoring agent in food products
Pharmacological activities
a. Anti-inflammatory properties
b. Analgesic properties
Check Digit Verification of cas no
The CAS Registry Mumber 7501-94-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7501-94:
(6*7)+(5*5)+(4*0)+(3*1)+(2*9)+(1*4)=92
92 % 10 = 2
So 7501-94-2 is a valid CAS Registry Number.
7501-94-2Relevant articles and documents
Diastereoselective friedel-crafts alkylation of indoles with chiral α-phenyl benzylic cations. Asymmetric synthesis of anti-1,1,2- triarylalkanes
Chung, John Y. L.,Mancheno, Danny,Dormer, Peter G.,Variankaval, Narayan,Ball, Richard G.,Tsou, Nancy N.
supporting information; experimental part, p. 3037 - 3040 (2009/05/07)
(Chemical Equation Presented) The reactions of chiral benzyl carbocations bearing α-phenyl substituents with N-sulfonylated indoles afford 1,1,2-triarylalkanes with antiselectivities. This outcome is a reversal of facial diastereoselectivity relative to B
