Cas 1201325-79-2,(S)-N-(4-methoxyphenyl)-N-(2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl)-(1-phenyl)propylamine

1201325-79-2

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Basic information

Product Name: (S)-N-(4-methoxyphenyl)-N-(2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl)-(1-phenyl)propylamine
Synonyms:
CAS NO:1201325-79-2
Molecular Formula:
Molecular Weight: 739.947
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: (S)-N-(4-methoxyphenyl)-N-(2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl)-(1-phenyl)propylamine(CAS DataBase Reference)
NIST Chemistry Reference: (S)-N-(4-methoxyphenyl)-N-(2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl)-(1-phenyl)propylamine(1201325-79-2)
EPA Substance Registry System: (S)-N-(4-methoxyphenyl)-N-(2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl)-(1-phenyl)propylamine(1201325-79-2)

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: 1201325-79-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1201325-79-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,3,2 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1201325-79:
(9*1)+(8*2)+(7*0)+(6*1)+(5*3)+(4*2)+(3*5)+(2*7)+(1*9)=92
92 % 10 = 2
So 1201325-79-2 is a valid CAS Registry Number.

1201325-79-2Upstream product

557-20-0 diethylzinc

1201325-79-2Downstream Products

3789-59-1 (R)-1-phenylpropylamine

1201325-79-2Relevant academic research and scientific papers

Stereoselective synthesis of α-arylalkylamines by glycosylation-induced asymmetric addition of organometallic compounds to imines

Allef, Petra,Kunz, Horst

, p. 646 - 652 (2009)

Activation of imines of aromatic aldehydes by N-glycosylation with O-pivaloyl-galactopyranosyl bromide (pivalobromogalactose) and subsequent addition of organotin, organolithium, Grignard, or organozinc reagents afforded α-arylalkylamines with moderate to

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