Cas 916751-09-2,(3S,4S,5R)-3-(trichloromethylcarbonylamino)-4-benzyl-5-methoxymethoxyhex-1-ene

916751-09-2

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Basic information

Product Name: (3S,4S,5R)-3-(trichloromethylcarbonylamino)-4-benzyl-5-methoxymethoxyhex-1-ene
Synonyms: (3S,4S,5R)-3-(trichloromethylcarbonylamino)-4-benzyl-5-methoxymethoxyhex-1-ene
CAS NO:916751-09-2
Molecular Formula:
Molecular Weight: 394.726
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: (3S,4S,5R)-3-(trichloromethylcarbonylamino)-4-benzyl-5-methoxymethoxyhex-1-ene(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4S,5R)-3-(trichloromethylcarbonylamino)-4-benzyl-5-methoxymethoxyhex-1-ene(916751-09-2)
EPA Substance Registry System: (3S,4S,5R)-3-(trichloromethylcarbonylamino)-4-benzyl-5-methoxymethoxyhex-1-ene(916751-09-2)

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: 916751-09-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 916751-09-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,7,5 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 916751-09:
(8*9)+(7*1)+(6*6)+(5*7)+(4*5)+(3*1)+(2*0)+(1*9)=182
182 % 10 = 2
So 916751-09-2 is a valid CAS Registry Number.

916751-09-2Upstream product

916751-03-6 C₁₇H₂₂Cl₃NO₃

916751-09-2Downstream Products

916751-13-8 (2S,3S,4R)-2-(trichloromethylcarbonylamino)-3-benzyl-4-methoxymethoxypentanoic acid

916751-09-2Relevant academic research and scientific papers

Stereocontrol of palladium(ii)-catalysed aza-Claisen rearrangements using a combination of 1,3-allylic strain and a solvent mediated directing effect

Swift, Michael D.,Sutherland, Andrew

, p. 3889 - 3891 (2008/09/18)

A non-coordination solvent was used for the aza-Claisen rearrangement of δ,ε-disubstituted acetimidates that generates a substrate directing effect, providing excellent stereoselectivity. The aza-Claisen rearrangement of allylic trichloroacetimidates was

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