Cas 1379113-75-3,methyl 3-((4R,5S)-2,2-dimethyl-5-((E)-pent-3-en-1-ynyl)-1,3-dioxolan-4-yl)propanoate

1379113-75-3

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Basic information

Product Name: methyl 3-((4R,5S)-2,2-dimethyl-5-((E)-pent-3-en-1-ynyl)-1,3-dioxolan-4-yl)propanoate
Synonyms: methyl 3-((4R,5S)-2,2-dimethyl-5-((E)-pent-3-en-1-ynyl)-1,3-dioxolan-4-yl)propanoate
CAS NO:1379113-75-3
Molecular Formula:
Molecular Weight: 252.31
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: methyl 3-((4R,5S)-2,2-dimethyl-5-((E)-pent-3-en-1-ynyl)-1,3-dioxolan-4-yl)propanoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 3-((4R,5S)-2,2-dimethyl-5-((E)-pent-3-en-1-ynyl)-1,3-dioxolan-4-yl)propanoate(1379113-75-3)
EPA Substance Registry System: methyl 3-((4R,5S)-2,2-dimethyl-5-((E)-pent-3-en-1-ynyl)-1,3-dioxolan-4-yl)propanoate(1379113-75-3)

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: 1379113-75-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1379113-75-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,1,1 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1379113-75:
(9*1)+(8*3)+(7*7)+(6*9)+(5*1)+(4*1)+(3*3)+(2*7)+(1*5)=173
173 % 10 = 3
So 1379113-75-3 is a valid CAS Registry Number.

1379113-75-3Upstream product

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1379113-75-3Relevant academic research and scientific papers

Total synthesis of sapinofuranone A from d-ribose

Nagarapu, Lingaiah,Karnakanti, Shuklachary,Bantu, Rajashaker

, p. 5829 - 5832 (2012)

The total synthesis of sapinofuranone A has been achieved starting from naturally occurring carbohydrate d-ribose via a short and high yielding route. The key transformations include Wittig olefination, Ohira-Bestmann reaction, Sonogashira coupling. Finally acetonide deprotection and subsequent lactonization using catalytic amount of hydrochloric acid completed the total synthesis of sapinofuranone A.

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