110167-20-9 Usage
General Description
4-BENZYL-3-HYDROXYMETHYLMORPHOLINE is a chemical compound with the molecular formula C14H19NO2. It is a morpholine derivative with a benzyl and hydroxymethyl group attached to the morpholine ring. This chemical is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It has potential applications in the production of medicines, such as anti-cancer drugs and anti-inflammatory agents. Additionally, its benzyl group makes it suitable for use as a building block in organic synthesis. 4-BENZYL-3-HYDROXYMETHYLMORPHOLINE is an important compound with versatile uses in the pharmaceutical and chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 110167-20-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,1,6 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 110167-20:
(8*1)+(7*1)+(6*0)+(5*1)+(4*6)+(3*7)+(2*2)+(1*0)=69
69 % 10 = 9
So 110167-20-9 is a valid CAS Registry Number.
110167-20-9Relevant articles and documents
FUSED THIAZOLE DERIVATIVES AS KINASE INHIBITORS
-
, (2008/06/13)
A series of 5,6-dihydro-l,3-benzothiazol-7(4H)-one derivatives, and analogues thereof, which are substituted in the 2-position by an optionally substituted morpholin-4-yl moiety, being selective inhibitors of PD kinase enzymes, are accordingly of b.enefit in medicine, for example in the treatment of inflammatory, autoimmune, cardiovascular, neurodegenerative, metabolic, oncological, nociceptive or ophthalmic conditions.
Chiral Synthesis of 3-Substituted Morpholines via Serine Enantiomers and Reductions of 5-Oxomorpholine-3-carboxylates
Brown, George R.,Foubister, Alan J.,Wright, Brian
, p. 2577 - 2580 (2007/10/02)
The chiral synthesis of 3-hydroxymethyl- and 3-carboxy-morpholines from serine enantiomers is described.Chemoselective and total reductions of 5-oxomorpholine-3-carboxylates are key synthetic steps.
