Cas 69797-31-5,β-(1-morpholinylmethyl)-β-benzoylpropionic acid

69797-31-5

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Basic information

Product Name: β-(1-morpholinylmethyl)-β-benzoylpropionic acid
Synonyms: β-(1-morpholinylmethyl)-β-benzoylpropionic acid
CAS NO:69797-31-5
Molecular Formula:
Molecular Weight: 277.32
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: β-(1-morpholinylmethyl)-β-benzoylpropionic acid(CAS DataBase Reference)
NIST Chemistry Reference: β-(1-morpholinylmethyl)-β-benzoylpropionic acid(69797-31-5)
EPA Substance Registry System: β-(1-morpholinylmethyl)-β-benzoylpropionic acid(69797-31-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 69797-31-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 69797-31-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,9 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69797-31:
(7*6)+(6*9)+(5*7)+(4*9)+(3*7)+(2*3)+(1*1)=195
195 % 10 = 5
So 69797-31-5 is a valid CAS Registry Number.

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69797-31-5Relevant academic research and scientific papers

Compound having effect of promoting neuron differentiation

-

, (2008/06/13)

A novel cystacycline derivative which has an excellent effect of promoting the differentiation of neurons and is useful as a remedy for central nervous system disorders, a remedy for peripheral nerve disorders, etc.

Synthesis of 3-aminomethyl-1-tetralones as potential neuroleptic agents

Eirin,Santana,Ravina,et al.

, p. 533 - 537 (2007/10/06)

3-Aminomethyl tetralones, which present the butyrophenone side chain partially incorporated in a semirigid structure have been prepared by Mannich reaction of β-benzoyl-propionic acids and heterocyclic amines, catalytic reduction of the carbonyl group and

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