Cas 37462-22-9,α,α-dimethyl-3,4-dimethoxyphenethylamine hydrochloride

37462-22-9

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Basic information

Product Name: α,α-dimethyl-3,4-dimethoxyphenethylamine hydrochloride
Synonyms: α,α-dimethyl-3,4-dimethoxyphenethylamine hydrochloride
CAS NO:37462-22-9
Molecular Formula:
Molecular Weight: 245.749
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: α,α-dimethyl-3,4-dimethoxyphenethylamine hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: α,α-dimethyl-3,4-dimethoxyphenethylamine hydrochloride(37462-22-9)
EPA Substance Registry System: α,α-dimethyl-3,4-dimethoxyphenethylamine hydrochloride(37462-22-9)

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: 37462-22-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 37462-22-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,4,6 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 37462-22:
(7*3)+(6*7)+(5*4)+(4*6)+(3*2)+(2*2)+(1*2)=119
119 % 10 = 9
So 37462-22-9 is a valid CAS Registry Number.

37462-22-9Upstream product

37462-22-9Downstream Products

37462-22-9Relevant academic research and scientific papers

1-DIPHENYLPHOSPHINYL-2,2-DIMETHYLAZIRIDINE - A NEW PRECURSOR OF α,α-DIMETHYLARYLALKYLAMINES

Buchowiecki, Wieslaw,Grosman-Zjawiona, Zofia,Zjawiony, Jordan

, p. 1245 - 1248 (2007/10/02)

The new synthesis of α,α-dimethylarylalkylamines from 1-diphenylphosphinyl-2,2-dimethylaziridine is described.

Novel benzylalcohol derivative and process for preparing the same

-

, (2008/06/13)

A benzylalcohol derivative of the formula: STR1 wherein R is hydroxy, benzyloxy, alkoxy of one to 4 carbon atoms or halogen, and Ring A is monomethoxyphenyl, dimethoxyphenyl, trimethoxyphenyl or 3,4-methylenedioxyphenyl is prepared by reducing a compound of the formula: STR2 wherein R' is benzyloxy, alkoxy of one to 4 carbon atoms or halogen, and Ring A is the same as defined above, and when R' is benzyloxy, if required, further subjecting the product to catalytic hydrogenation. The compounds (I) and pharmaceutically acceptable acid addition salts thereof are used as anti-diabetic agents.

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