943443-05-8 Usage
Uses
Used in Pharmaceutical Industry:
(S)-4-benzyl-1,4-oxazepan-6-ol is utilized as a precursor in the synthesis of bioactive molecules for various therapeutic applications. Its unique structure and chirality allow for the development of new drugs with specific targeting and efficacy profiles.
Used in Drug Discovery:
As a building block in drug discovery, (S)-4-benzyl-1,4-oxazepan-6-ol contributes to the creation of novel chemical entities with potential medicinal properties. Its incorporation into drug candidates can lead to the discovery of new treatments for a range of diseases and conditions.
Used in Medicinal Chemistry Research and Development:
(S)-4-benzyl-1,4-oxazepan-6-ol serves as a valuable compound in medicinal chemistry research and development. Its unique structural features and chirality make it an ideal candidate for exploring the relationship between chemical structure and biological activity, ultimately aiding in the advancement of pharmaceutical science.
Check Digit Verification of cas no
The CAS Registry Mumber 943443-05-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,4,4 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 943443-05:
(8*9)+(7*4)+(6*3)+(5*4)+(4*4)+(3*3)+(2*0)+(1*5)=168
168 % 10 = 8
So 943443-05-8 is a valid CAS Registry Number.
943443-05-8Relevant articles and documents
PROCESS FOR PRODUCING 2-HYDROXYMETHYLMORPHOLINE SALT
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Page/Page column 13-14, (2011/12/03)
The present invention relates to a production method of a 2-hydroxymethylmorpholine salt, which includes crystallization from a solution containing 2-hydroxymethylmorpholine represented by the following formula (1) 1,4-oxazepane compound represented by th
Concise synthesis of (S)-N-BOC-2-hydroxymethylmorpholine and (S)-N-BOC-morpholine-2-carboxylic acid
Henegar, Kevin E.
, p. 3662 - 3665 (2008/09/20)
(Chemical Equation Presented) An operationally simple synthesis of N-BOC-2-hydroxymethylmorpholine (1) and N-BOC-morpholine-2-carboxylic acid (2) from epichlorohydrin has been developed. No chromatography is required in the processing, which allows high p
Efficient one-pot synthesis of enantiomerically pure 2-(hydroxymethyl)- morpholines
Breuning, Matthias,Winnacker, Malte,Steiner, Melanie
, p. 2100 - 2106 (2008/02/06)
An efficient and convenient one-pot procedure for the synthesis of enantiomerically pure 2-(hydroxymethyl)morpholines with a widely variable substitution pattern was developed. Addition of chiral β-amino alcohols to (S)- or (R)-epichlorohydrin in the pres
