Cas 1058728-79-2,(2S,3S,6S)-6-[((1S,2S)-allyloxyethyl)-but-3-enyloxy]-3-benzyloxy-2-methyltetrahydropyran

1058728-79-2

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Basic information

Product Name: (2S,3S,6S)-6-[((1S,2S)-allyloxyethyl)-but-3-enyloxy]-3-benzyloxy-2-methyltetrahydropyran
Synonyms: (2S,3S,6S)-6-[((1S,2S)-allyloxyethyl)-but-3-enyloxy]-3-benzyloxy-2-methyltetrahydropyran
CAS NO:1058728-79-2
Molecular Formula:
Molecular Weight: 360.494
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: (2S,3S,6S)-6-[((1S,2S)-allyloxyethyl)-but-3-enyloxy]-3-benzyloxy-2-methyltetrahydropyran(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S,6S)-6-[((1S,2S)-allyloxyethyl)-but-3-enyloxy]-3-benzyloxy-2-methyltetrahydropyran(1058728-79-2)
EPA Substance Registry System: (2S,3S,6S)-6-[((1S,2S)-allyloxyethyl)-but-3-enyloxy]-3-benzyloxy-2-methyltetrahydropyran(1058728-79-2)

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: 1058728-79-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1058728-79-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,8,7,2 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1058728-79:
(9*1)+(8*0)+(7*5)+(6*8)+(5*7)+(4*2)+(3*8)+(2*7)+(1*9)=182
182 % 10 = 2
So 1058728-79-2 is a valid CAS Registry Number.

1058728-79-2Upstream product

1058728-79-2Downstream Products

1058728-81-6 (2S,3S)-3-((2S,5S,6S)-5-benzyloxy-6-methyltetrahydropyran-2-yloxy)-2-methyl-2,3,4,5-tetrahydrooxepine

1058728-79-2Relevant academic research and scientific papers

The tandem ring-closing metathesis-isomerization approach to 6-deoxyglycals

Schmidt, Bernd,Biernat, Anne

, p. 6135 - 6141 (2008)

Protected 3,6-dideoxyglycals have been synthesized de novo as single isomers starting from ethyl lactate by using the tandem RCM-isomerization reaction as the key step. Different relative configurations become accessible by addition of vinyl- or allylmeta

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