149177-75-3 Usage
Uses
Used in Organic Synthesis:
(2R)-3,4-dihydro-2H-chromen-2-ylmethylamine hydrochloride is utilized as a key intermediate in organic synthesis, contributing to the formation of complex organic molecules and facilitating the development of new chemical entities.
Used in Chemical Reactions as a Reagent:
As a reagent, (2R)-3,4-dihydro-2H-chromen-2-ylmethylamine hydrochloride is employed to catalyze or participate in various chemical reactions, aiding in the production of desired products and enhancing the efficiency of these processes.
Used in Pharmaceutical Research and Development:
(2R)-3,4-dihydro-2H-chromen-2-ylmethylamine hydrochloride may have potential applications in the pharmaceutical industry, where it could be explored for its properties and uses in the development of new drugs and therapeutic agents.
Used in Agrochemicals:
In the agrochemical sector, (2R)-3,4-dihydro-2H-chromen-2-ylmethylamine hydrochloride could be investigated for its potential use in the development of pesticides, herbicides, or other agricultural chemicals, contributing to more effective and sustainable agricultural practices.
Used in Materials Science:
(2R)-3,4-dihydro-2H-chromen-2-ylmethylamine hydrochloride may also find applications in materials science, where its unique properties could be harnessed to create new materials with specific characteristics for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 149177-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,1,7 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 149177-75:
(8*1)+(7*4)+(6*9)+(5*1)+(4*7)+(3*7)+(2*7)+(1*5)=163
163 % 10 = 3
So 149177-75-3 is a valid CAS Registry Number.
149177-75-3Relevant academic research and scientific papers
CHROMANE AND CHROMENE DERIVATIVES AND USES THEREOF
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Page/Page column 79, (2010/11/28)
Methods of preparing compounds of formula (I) or pharmaceutically acceptable salts thereof are provided wherein each of R1, R2, R3, R4, x, m, n, and Ar are as defined, and described in classes and subclasses herein, which are agonists or partial agonists of the 2C subtype of brain serotonin receptors. The compounds, and compositions containing the compounds, can be used to treat a variety of central nervous system disorders such as schizophrenia.
METHOD FOR PRODUCING CHROMANE DERIVATIVES THAT ARE DEVOID OF ENANTIOMERS AND ARE SUBSTITUTED IN POSITION 2
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Page/Page column 12, (2008/06/13)
The invention relates to a method for producing chromane derivatives that are devoid of enantiomers and are substituted in position 2, from corresponding chromane-2-carboxylic acid esters.
Synthesis of optically active 6-substituted 2-(aminomethyl)chromans
Zhang, Mingbao,Reeves, Raymond,Bi, Cheng,Dally, Robert,Ladouceur, Gaetan,Bullock, William,Chin, Jefferson
, p. 5229 - 5231 (2007/10/03)
Three novel, optically active, 6-substituted 2-(aminomethyl)chromans were synthesized from readily available chroman 2-carboxylic acid precursors. These chroman-containing primary amines are useful building blocks for the synthesis of chroman-derived phar
