1173110-88-7 Usage
General Description
(R)-3-Methyl-1-Phenylbutan-1-amine hydrochloride, also known as modular AMPA receptor positive allosteric modulator 4, is an organically synthesized compound that belongs to the alpha-branched primary amines, characterized by a primary amino group connected to an alpha-carbon with one or more substitutions. (R)-3-METHYL-1-PHENYLBUTAN-1-AMINE-HCl has a molecular weight of 227.74 and a molecular formula of C11H17NHCl. Its chemical structure includes an AMINE group attached to a 3-methyl-1-phenylbutan group. Being a hydrochloride, it is an acidic salt made from the reaction of this amine with hydrochloric acid. (R)-3-METHYL-1-PHENYLBUTAN-1-AMINE-HCl may have biologically active properties but is primarily used for research purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 1173110-88-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,1,1 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1173110-88:
(9*1)+(8*1)+(7*7)+(6*3)+(5*1)+(4*1)+(3*0)+(2*8)+(1*8)=117
117 % 10 = 7
So 1173110-88-7 is a valid CAS Registry Number.
1173110-88-7Relevant articles and documents
Method for synthesizing chiral amine compound
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Paragraph 0084; 0091-0093, (2019/10/01)
The present invention provides a method for synthesizing a chiral amine compound. The method comprises the following steps: (1) reacting a compound of formula I with t-butylsulfonamide in the presenceof a catalyst to obtain a compound having a structure represented by formula II; 2) reacting the compound of the formula II in a hydrogen atmosphere in the presence of an iridium catalyst and a ligand to obtain a compound of formula III; and (3) carrying out a t-butylsulfonyl group removal reaction on the compound of the formula III to obtain the chiral amine compound. The method constructs the structure of sulfonamide by a keto carbonylgroup, and synthesizes the chiral amine compound with the aralkylamine structure by an asymmetric catalytic hydrogenation reaction of the sulfonamide structure, the ee value is generally 80% or above, the highest ee value is 99% or above, the yield of each step reaction can reach 90% or above, and the total yield is high.
