Cas 163625-40-9,(2S,3R)-(E)-N<sup>α</sup>-(tert-Butoxycarbonyl)-N-methoxy-N-methyl-2-amino-6-(benzyloxy)-3-hydroxy-4-hexenamide

163625-40-9

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Basic information

Product Name: (2S,3R)-(E)-N^α-(tert-Butoxycarbonyl)-N-methoxy-N-methyl-2-amino-6-(benzyloxy)-3-hydroxy-4-hexenamide
Synonyms: (2S,3R)-(E)-N^α-(tert-Butoxycarbonyl)-N-methoxy-N-methyl-2-amino-6-(benzyloxy)-3-hydroxy-4-hexenamide
CAS NO:163625-40-9
Molecular Formula:
Molecular Weight: 394.468
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: (2S,3R)-(E)-N^α-(tert-Butoxycarbonyl)-N-methoxy-N-methyl-2-amino-6-(benzyloxy)-3-hydroxy-4-hexenamide(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3R)-(E)-N^α-(tert-Butoxycarbonyl)-N-methoxy-N-methyl-2-amino-6-(benzyloxy)-3-hydroxy-4-hexenamide(163625-40-9)
EPA Substance Registry System: (2S,3R)-(E)-N^α-(tert-Butoxycarbonyl)-N-methoxy-N-methyl-2-amino-6-(benzyloxy)-3-hydroxy-4-hexenamide(163625-40-9)

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: 163625-40-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 163625-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,6,2 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 163625-40:
(8*1)+(7*6)+(6*3)+(5*6)+(4*2)+(3*5)+(2*4)+(1*0)=129
129 % 10 = 9
So 163625-40-9 is a valid CAS Registry Number.

163625-40-9Upstream product

163625-40-9Downstream Products

163625-45-4 (4S,5R)-5-<(E)-3-(Benzyloxy)-1-propenyl>-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-(N-methoxy-N-methylcarbamoyl)oxazolidine

163625-40-9Relevant academic research and scientific papers

Gold(I)-Catalyzed Asymmetric Aldol Reaction of N-Methoxy-N-methyl-α-isocyanoacetamide (α-Isocyano Weinreb Amide). An Efficient Synthesis of Optically Active β-Hydroxy α-Amino Aldehydes and Ketones

Sawamura, Masaya,Nakayama, Yuki,Kato, Tomoki,Ito, Yoshihiko

, p. 1727 - 1732 (2007/10/02)

Asymmetric aldol reaction of N-methoxy-N-methyl-α-isocyanoacetamide (α-isocyano Weinreb amide) with aldehydes in the presence of a gold(I) catalyst prepared in situ from BF4 and chiral fe

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