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(+/-)-Threo-3-amino-2,3-diphenyl-1-propanol, also known as Threo-DOPS or (+/-)-3-amino-2,3-diphenyl-1-propanol, is a chiral amino alcohol with the molecular formula C15H17NO. It is a white crystalline solid that is soluble in water and various organic solvents. (+/-)-threo-3-amino-2,3-diphenyl-1-propanol is of interest in the field of pharmaceuticals and organic chemistry due to its potential applications as a precursor in the synthesis of various drugs and as a chiral auxiliary in asymmetric synthesis. The threo configuration refers to the relative positions of the substituents on the chiral carbon atoms, which can significantly influence the compound's biological activity and reactivity. The presence of the amino group and the diphenyl group gives this molecule unique properties that can be exploited in the design of new pharmaceuticals and other chemical products.

6476-89-7

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6476-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6476-89-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,7 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6476-89:
(6*6)+(5*4)+(4*7)+(3*6)+(2*8)+(1*9)=127
127 % 10 = 7
So 6476-89-7 is a valid CAS Registry Number.

6476-89-7Downstream Products

6476-89-7Relevant academic research and scientific papers

Organocatalytic Mannich-type reactions of trifluoroethyl thioesters

Utsumi, Naoto,Kitagaki, Shinji,Barbas III, Carlos F.

supporting information; experimental part, p. 3405 - 3408 (2009/04/21)

(Chemical Equation Presented) Direct organocatalytic Mannich-type reactions of thioesters provide for the expedient and diastereoselective synthesis of protected β-amino acids. A variety of thioesters were found to be reactive with different lmines under mild conditions to provide β-amino acids in good yields. This chemistry was extended to a diastereo- and enantioselective variant.

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