Cas 319432-63-8,((Z)-(1R,5R,10R,11S,12R,13S)-11,12,13-Tris-benzyloxy-4-oxo-3,14-dioxa-bicyclo[8.3.1]tetradec-7-en-5-yl)-carbamic acid tert-butyl ester

319432-63-8

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Basic information

Product Name: ((Z)-(1R,5R,10R,11S,12R,13S)-11,12,13-Tris-benzyloxy-4-oxo-3,14-dioxa-bicyclo[8.3.1]tetradec-7-en-5-yl)-carbamic acid tert-butyl ester
Synonyms: ((Z)-(1R,5R,10R,11S,12R,13S)-11,12,13-Tris-benzyloxy-4-oxo-3,14-dioxa-bicyclo[8.3.1]tetradec-7-en-5-yl)-carbamic acid tert-butyl ester
CAS NO:319432-63-8
Molecular Formula:
Molecular Weight: 643.777
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: ((Z)-(1R,5R,10R,11S,12R,13S)-11,12,13-Tris-benzyloxy-4-oxo-3,14-dioxa-bicyclo[8.3.1]tetradec-7-en-5-yl)-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: ((Z)-(1R,5R,10R,11S,12R,13S)-11,12,13-Tris-benzyloxy-4-oxo-3,14-dioxa-bicyclo[8.3.1]tetradec-7-en-5-yl)-carbamic acid tert-butyl ester(319432-63-8)
EPA Substance Registry System: ((Z)-(1R,5R,10R,11S,12R,13S)-11,12,13-Tris-benzyloxy-4-oxo-3,14-dioxa-bicyclo[8.3.1]tetradec-7-en-5-yl)-carbamic acid tert-butyl ester(319432-63-8)

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: 319432-63-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 319432-63-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,9,4,3 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 319432-63:
(8*3)+(7*1)+(6*9)+(5*4)+(4*3)+(3*2)+(2*6)+(1*3)=138
138 % 10 = 8
So 319432-63-8 is a valid CAS Registry Number.

319432-63-8Upstream product

319432-63-8Downstream Products

319432-68-3 (Z)-(R)-2-tert-Butoxycarbonylamino-6-((2R,3S,4R,5S,6R)-3,4,5-tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-hex-4-enoic acid methyl ester

319432-63-8Relevant academic research and scientific papers

Facile synthesis of building blocks for C-glycosidic neoglycoconjugates

Walter,Westermann

, p. 1682 - 1684 (2007/10/03)

Highly functionalized C-glycosidic neoglycoconjugate building blocks can be synthesized via an intramolecular ring closing olefin metathesis reaction (RCM). The products can be formed α- and β-selectively while starting from their allylated congeners. Due to the intramolecular approach, the RCM is cis-selective leading to cyclized products in high yields. Furthermore, attachment to polymeric resins may allow solid phase synthesis.

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