Cas 220206-35-9,(2R,4aR,7R,8R,8aR)-7,8-Bis-benzyloxy-2-phenyl-4a,7,8,8a-tetrahydro-4H-benzo[1,3]dioxine

220206-35-9

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Basic information

Product Name: (2R,4aR,7R,8R,8aR)-7,8-Bis-benzyloxy-2-phenyl-4a,7,8,8a-tetrahydro-4H-benzo[1,3]dioxine
Synonyms: (2R,4aR,7R,8R,8aR)-7,8-Bis-benzyloxy-2-phenyl-4a,7,8,8a-tetrahydro-4H-benzo[1,3]dioxine
CAS NO:220206-35-9
Molecular Formula:
Molecular Weight: 428.528
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: (2R,4aR,7R,8R,8aR)-7,8-Bis-benzyloxy-2-phenyl-4a,7,8,8a-tetrahydro-4H-benzo[1,3]dioxine(CAS DataBase Reference)
NIST Chemistry Reference: (2R,4aR,7R,8R,8aR)-7,8-Bis-benzyloxy-2-phenyl-4a,7,8,8a-tetrahydro-4H-benzo[1,3]dioxine(220206-35-9)
EPA Substance Registry System: (2R,4aR,7R,8R,8aR)-7,8-Bis-benzyloxy-2-phenyl-4a,7,8,8a-tetrahydro-4H-benzo[1,3]dioxine(220206-35-9)

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: 220206-35-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 220206-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,2,0 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 220206-35:
(8*2)+(7*2)+(6*0)+(5*2)+(4*0)+(3*6)+(2*3)+(1*5)=69
69 % 10 = 9
So 220206-35-9 is a valid CAS Registry Number.

220206-35-9Upstream product

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220206-35-9Relevant academic research and scientific papers

Synthesis of bicyclic derivatives of 5A-carbasugars: 6-Hydroxyl group conformationally restricted 5A-carba-D-mannopyranose derivatives

Ogawa, Seiichiro,Ohno, Masatsugu,Ohhira, Takashi

, p. 57 - 62 (2007/10/03)

Some bicyclic derivatives of 5a-carba-α-and β-D-mannopyranoses, whose 6-hydroxyl groups are conformationally restricted, have been synthesized in order to provide key components of the trisaccharide mimics designed as inhibitors or substrate analogues use

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