Cas 634584-42-2,tert-butyl (3aR,4S,6aS)-4-{[([1,1'-biphenyl]-4-ylmethyl)amino]methyl}tetrahydro-2,2-dimethyl-5H-[1,3]dioxolo[4,5-c]pyrrole-5-carboxylate

634584-42-2

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Product Name: tert-butyl (3aR,4S,6aS)-4-{[([1,1'-biphenyl]-4-ylmethyl)amino]methyl}tetrahydro-2,2-dimethyl-5H-[1,3]dioxolo[4,5-c]pyrrole-5-carboxylate
Synonyms: tert-butyl (3aR,4S,6aS)-4-{[([1,1'-biphenyl]-4-ylmethyl)amino]methyl}tetrahydro-2,2-dimethyl-5H-[1,3]dioxolo[4,5-c]pyrrole-5-carboxylate
CAS NO:634584-42-2
Molecular Formula:
Molecular Weight: 438.567
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: tert-butyl (3aR,4S,6aS)-4-{[([1,1'-biphenyl]-4-ylmethyl)amino]methyl}tetrahydro-2,2-dimethyl-5H-[1,3]dioxolo[4,5-c]pyrrole-5-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (3aR,4S,6aS)-4-{[([1,1'-biphenyl]-4-ylmethyl)amino]methyl}tetrahydro-2,2-dimethyl-5H-[1,3]dioxolo[4,5-c]pyrrole-5-carboxylate(634584-42-2)
EPA Substance Registry System: tert-butyl (3aR,4S,6aS)-4-{[([1,1'-biphenyl]-4-ylmethyl)amino]methyl}tetrahydro-2,2-dimethyl-5H-[1,3]dioxolo[4,5-c]pyrrole-5-carboxylate(634584-42-2)

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: 634584-42-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 634584-42-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,4,5,8 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 634584-42:
(8*6)+(7*3)+(6*4)+(5*5)+(4*8)+(3*4)+(2*4)+(1*2)=172
172 % 10 = 2
So 634584-42-2 is a valid CAS Registry Number.

634584-42-2Upstream product

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634584-42-2Relevant academic research and scientific papers

Synthesis and α-mannosidase inhibitory evaluation of (2R,3R,4S)- and (2S,3R,4S)-2-(aminomethyl)pyrrolidine-3,4-diol derivatives

Popowycz, Florence,Gerber-Lemaire, Sandrine,Rodriguez-Garcia, Eliazar,Schuetz, Catherine,Vogel, Pierre

, p. 1914 - 1948 (2007/10/03)

The synthesis of 46 derivatives of (2R,3R,4S)-2-(aminomethyl)pyrrolidine-3,4-diol is reported (Scheme 1 and Fig. 3), and their inhibitory activities toward α-mannosidases from jack bean (B) and almonds (A) are evaluated (Table). The most-potent inhibitors

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