Cas 852713-56-5,(3R,4aS,5R,6S,11bR,11cS)-5-Benzyloxy-11b,11c-dihydroxy-6-hydroxymethyl-3-phenyl-5,6,11b,11c-tetrahydro-1H,4aH-2,4-dioxa-6a-aza-benzo[c]fluoren-7-one

852713-56-5

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Basic information

Product Name: (3R,4aS,5R,6S,11bR,11cS)-5-Benzyloxy-11b,11c-dihydroxy-6-hydroxymethyl-3-phenyl-5,6,11b,11c-tetrahydro-1H,4aH-2,4-dioxa-6a-aza-benzo[c]fluoren-7-one
Synonyms: (3R,4aS,5R,6S,11bR,11cS)-5-Benzyloxy-11b,11c-dihydroxy-6-hydroxymethyl-3-phenyl-5,6,11b,11c-tetrahydro-1H,4aH-2,4-dioxa-6a-aza-benzo[c]fluoren-7-one
CAS NO:852713-56-5
Molecular Formula:
Molecular Weight: 489.525
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,4aS,5R,6S,11bR,11cS)-5-Benzyloxy-11b,11c-dihydroxy-6-hydroxymethyl-3-phenyl-5,6,11b,11c-tetrahydro-1H,4aH-2,4-dioxa-6a-aza-benzo[c]fluoren-7-one(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4aS,5R,6S,11bR,11cS)-5-Benzyloxy-11b,11c-dihydroxy-6-hydroxymethyl-3-phenyl-5,6,11b,11c-tetrahydro-1H,4aH-2,4-dioxa-6a-aza-benzo[c]fluoren-7-one(852713-56-5)
EPA Substance Registry System: (3R,4aS,5R,6S,11bR,11cS)-5-Benzyloxy-11b,11c-dihydroxy-6-hydroxymethyl-3-phenyl-5,6,11b,11c-tetrahydro-1H,4aH-2,4-dioxa-6a-aza-benzo[c]fluoren-7-one(852713-56-5)

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: 852713-56-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 852713-56-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,7,1 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 852713-56:
(8*8)+(7*5)+(6*2)+(5*7)+(4*1)+(3*3)+(2*5)+(1*6)=175
175 % 10 = 5
So 852713-56-5 is a valid CAS Registry Number.

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852713-56-5Relevant academic research and scientific papers

Ketone-imide versus ketone-oxime reductive cross-coupling promoted by samarium diiodide: New mechanistic insight gained from a failed aminocyclopentitol synthesis

Chiara, Jose Luis,Garcia, Angela,Cristobal-Lumbroso, Gabriella

, p. 4142 - 4151 (2007/10/03)

The intramolecular 1,6-ketone/imide reductive coupling promoted by samarium diiodide competes favorably with an alternative 1,5-ketone/oxime ether coupling in a keto-oxime substrate derived from D-glucosamine N-protected with a phthalimido group. This pin

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