Cas 1219706-22-5,(1S,5R,6R,4'S)-4-benzyl-7,7-dibromo-5-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-6-methoxy-3-oxa-4-azabicyclo[4.1.0]heptane

1219706-22-5

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Basic information

Product Name: (1S,5R,6R,4'S)-4-benzyl-7,7-dibromo-5-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-6-methoxy-3-oxa-4-azabicyclo[4.1.0]heptane
Synonyms:
CAS NO:1219706-22-5
Molecular Formula:
Molecular Weight: 477.193
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: (1S,5R,6R,4'S)-4-benzyl-7,7-dibromo-5-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-6-methoxy-3-oxa-4-azabicyclo[4.1.0]heptane(CAS DataBase Reference)
NIST Chemistry Reference: (1S,5R,6R,4'S)-4-benzyl-7,7-dibromo-5-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-6-methoxy-3-oxa-4-azabicyclo[4.1.0]heptane(1219706-22-5)
EPA Substance Registry System: (1S,5R,6R,4'S)-4-benzyl-7,7-dibromo-5-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-6-methoxy-3-oxa-4-azabicyclo[4.1.0]heptane(1219706-22-5)

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: 1219706-22-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1219706-22-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,9,7,0 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1219706-22:
(9*1)+(8*2)+(7*1)+(6*9)+(5*7)+(4*0)+(3*6)+(2*2)+(1*2)=145
145 % 10 = 5
So 1219706-22-5 is a valid CAS Registry Number.

1219706-22-5Upstream product

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1219706-22-5Relevant 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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