736991-35-8 Usage
General Description
3-Fluoro-2-(N-morpholino)-benzaldehyde is a chemical compound with the molecular formula C9H9FNO2. It is a benzaldehyde derivative with a fluorine atom at the 3-position and a N-morpholino group at the 2-position. 3-FLUORO-2-(N-MORPHOLINO)-BENZALDEHYDE is commonly used in the synthesis of pharmaceuticals and agrochemicals as a building block. Its unique structure and properties make it a valuable intermediate for the production of various organic compounds, and it has potential applications in the development of new drugs and materials. Additionally, 3-Fluoro-2-(N-morpholino)-benzaldehyde may also be used in research and development in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 736991-35-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,6,9,9 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 736991-35:
(8*7)+(7*3)+(6*6)+(5*9)+(4*9)+(3*1)+(2*3)+(1*5)=208
208 % 10 = 8
So 736991-35-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H12FNO2/c12-10-3-1-2-9(8-14)11(10)13-4-6-15-7-5-13/h1-3,8H,4-7H2
736991-35-8Relevant articles and documents
CARBAMATE COMPOUNDS AND OF MAKING AND USING SAME
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Paragraph 00187, (2013/07/19)
This disclosure provides compounds and compositions which may be modulators of MAGL and/or ABHD6 and their use as medicinal agents, processes for their preparation, and pharmaceutical compositions that include disclosed compunds as at least one active agent. The disclosure also provides for method of treating a patient in need thereof, where the patient is suffering from indications such as pain, solid tumor cancer and/or obesity comprising administering a disclosed compound or composition.
Scope and limitations of the T-reaction employing some functionalized C-H-acids and naturally occurring secondary amines
Rabong, Constantin,Hametner, Christian,Mereiter, Kurt,Kartsev, Victor G.,Jordis, Ulrich
, p. 799 - 838 (2008/09/21)
Scope and limitations of the T-reaction with emphasis on using chiral, natural products as starting materials to prepare novel chiral heterocycles is studied and the diastereoselective introduction of newly formed stereocenters is explained via proposed mechanisms.