Cas 1418476-85-3,tert-butyl ((3R,5R)-5-(((benzyloxy)carbonyl)oxy)-6,6-dimethylhept-1-en-3-yl)carbamate

1418476-85-3

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Basic information

Product Name: tert-butyl ((3R,5R)-5-(((benzyloxy)carbonyl)oxy)-6,6-dimethylhept-1-en-3-yl)carbamate
Synonyms: tert-butyl ((3R,5R)-5-(((benzyloxy)carbonyl)oxy)-6,6-dimethylhept-1-en-3-yl)carbamate
CAS NO:1418476-85-3
Molecular Formula:
Molecular Weight: 391.508
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: tert-butyl ((3R,5R)-5-(((benzyloxy)carbonyl)oxy)-6,6-dimethylhept-1-en-3-yl)carbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl ((3R,5R)-5-(((benzyloxy)carbonyl)oxy)-6,6-dimethylhept-1-en-3-yl)carbamate(1418476-85-3)
EPA Substance Registry System: tert-butyl ((3R,5R)-5-(((benzyloxy)carbonyl)oxy)-6,6-dimethylhept-1-en-3-yl)carbamate(1418476-85-3)

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: 1418476-85-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1418476-85-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,8,4,7 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1418476-85:
(9*1)+(8*4)+(7*1)+(6*8)+(5*4)+(4*7)+(3*6)+(2*8)+(1*5)=183
183 % 10 = 3
So 1418476-85-3 is a valid CAS Registry Number.

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1418476-85-3Relevant academic research and scientific papers

Concise asymmetric synthesis of orthogonally protected syn - And anti -1,3-aminoalcohols

Lee, Jae Seung,Kim, Dongeun,Lozano, Lucia,Kong, Suk Bin,Han, Hyunsoo

, p. 554 - 557 (2013)

Novel chiral binfunctional reagents V and ent-V undergo asymmetric aldehyde allylation followed by Ir(I)-catalyzed enantioselective allylic amidation to give orthogonally protected syn- and anti-1,3-aminoalcohols with complete control of absolute and rela

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