Cas 869368-04-7,(3R,4'S)-3-{2-benzyl-4,4-dimethoxy-3-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-2,3,4,7-tetrahydro[1,2]oxazepin-5-yl}acrylic acid methyl ester

869368-04-7

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Basic information

Product Name: (3R,4'S)-3-{2-benzyl-4,4-dimethoxy-3-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-2,3,4,7-tetrahydro[1,2]oxazepin-5-yl}acrylic acid methyl ester
Synonyms: (3R,4'S)-3-{2-benzyl-4,4-dimethoxy-3-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-2,3,4,7-tetrahydro[1,2]oxazepin-5-yl}acrylic acid methyl ester
CAS NO:869368-04-7
Molecular Formula:
Molecular Weight: 433.502
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: (3R,4'S)-3-{2-benzyl-4,4-dimethoxy-3-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-2,3,4,7-tetrahydro[1,2]oxazepin-5-yl}acrylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4'S)-3-{2-benzyl-4,4-dimethoxy-3-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-2,3,4,7-tetrahydro[1,2]oxazepin-5-yl}acrylic acid methyl ester(869368-04-7)
EPA Substance Registry System: (3R,4'S)-3-{2-benzyl-4,4-dimethoxy-3-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-2,3,4,7-tetrahydro[1,2]oxazepin-5-yl}acrylic acid methyl ester(869368-04-7)

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: 869368-04-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 869368-04-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,3,6 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 869368-04:
(8*8)+(7*6)+(6*9)+(5*3)+(4*6)+(3*8)+(2*0)+(1*4)=227
227 % 10 = 7
So 869368-04-7 is a valid CAS Registry Number.

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869368-04-7Relevant academic research and scientific papers

Ring enlargement of carbohydrate-derived 1,2-Oxazines to enantiopure 5-Bromo-1,2-oxazepines and subsequent palladium-catalyzed reactions

Al-Harrasi, Ahmed,Fischer, Sebastian,Zimmer, Reinhold,Reissig, Hans-Ulrich

experimental part, p. 304 - 314 (2010/04/03)

Dibromocarbene addition to d-glyceraldehyde-derived 1,2-oxazines syn-1 and anti-1 provided dibromocyclopropane intermediates syn-3 and anti-3, which smoothly reacted with methanol under ring enlargement to furnish 5-bromo-1,2-oxazepine derivatives syn-4 a

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