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(2R,3R)-3-aminopentan-2-ol hydrochloride is a chemical compound with the molecular formula C5H13NO. It is an amino alcohol, which means it contains both amine and alcohol functional groups. (2R,3R)-3-aminopentan-2-ol hydrochloride is commonly used in organic synthesis and pharmaceutical research due to its versatile reactivity and potential therapeutic applications. As a hydrochloride salt, it is more stable and soluble in water, making it easier to handle and use in various experimental setups. The stereochemistry of the compound is defined by the (2R,3R) prefix, indicating the arrangement of substituents around the chiral centers. (2R,3R)-3-aminopentan-2-ol hydrochloride has potential applications as a precursor in the synthesis of various pharmaceuticals and as a chiral building block in organic chemistry.

951000-34-3

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951000-34-3 Usage

Uses

Used in Pharmaceutical Research:
(2R,3R)-3-aminopentan-2-ol hydrochloride is used as a precursor in the synthesis of various pharmaceuticals for its versatile reactivity and potential therapeutic applications.
Used in Organic Chemistry:
(2R,3R)-3-aminopentan-2-ol hydrochloride is used as a chiral building block in organic chemistry for its unique stereochemistry and ability to facilitate the creation of enantioselective compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 951000-34-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,1,0,0 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 951000-34:
(8*9)+(7*5)+(6*1)+(5*0)+(4*0)+(3*0)+(2*3)+(1*4)=123
123 % 10 = 3
So 951000-34-3 is a valid CAS Registry Number.

951000-34-3Relevant academic research and scientific papers

TRPV3 Modulators

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Page/Page column 54, (2012/10/08)

Disclosed herein are modulators of TRPV3 of formula (I) wherein X1, X2, R1, R2, Rx, and n are as defined in the specification. Compositions comprising such compounds and methods for treating conditions and disorders using such compounds and compositions are also presented.

Stereoselective Synthesis of 1,2-Disubstituted β-Amino Alcohols by Nucleophilic Addition to N-tert-Butanesulfinyl α-Alkoxyaldimines

Evans, Jared W.,Ellman, Jonathan A.

, p. 9948 - 9957 (2007/10/03)

N-tert-Butanesulfinyl α-alkoxyaldimines are readily prepared from protected (S)-lactals without epimerization at the α-stereocenter. Addition of ethyl and phenyl Grignard reagents, as well as the titanium enolate of methyl acetate, to the N-tert-butanesul

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