Cas 677751-95-0,Spiro[1,3-dioxolane-4,2-[6]oxabicyclo[3.1.0]hexane], 2,2,5,5-tetramethyl-, (1R,2R,5S,5R)- (9CI)

677751-95-0

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Basic information

Product Name: Spiro[1,3-dioxolane-4,2-[6]oxabicyclo[3.1.0]hexane], 2,2,5,5-tetramethyl-, (1R,2R,5S,5R)- (9CI)
Synonyms: Spiro[1,3-dioxolane-4,2-[6]oxabicyclo[3.1.0]hexane], 2,2,5,5-tetramethyl-, (1R,2R,5S,5R)- (9CI)
CAS NO:677751-95-0
Molecular Formula: C11H18O3
Molecular Weight: 198.25882
EINECS: N/A
Product Categories: CYCLOPENTANE
Mol File: 677751-95-0.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Spiro[1,3-dioxolane-4,2-[6]oxabicyclo[3.1.0]hexane], 2,2,5,5-tetramethyl-, (1R,2R,5S,5R)- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Spiro[1,3-dioxolane-4,2-[6]oxabicyclo[3.1.0]hexane], 2,2,5,5-tetramethyl-, (1R,2R,5S,5R)- (9CI)(677751-95-0)
EPA Substance Registry System: Spiro[1,3-dioxolane-4,2-[6]oxabicyclo[3.1.0]hexane], 2,2,5,5-tetramethyl-, (1R,2R,5S,5R)- (9CI)(677751-95-0)

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: 677751-95-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 677751-95-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,7,7,5 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 677751-95:
(8*6)+(7*7)+(6*7)+(5*7)+(4*5)+(3*1)+(2*9)+(1*5)=220
220 % 10 = 0
So 677751-95-0 is a valid CAS Registry Number.

677751-95-0Upstream product

677752-04-4 (4S,5S)-2,2,4,7-Tetramethyl-1,3-dioxa-spiro[4.4]non-6-ene

677751-95-0Downstream Products

677751-95-0Relevant academic research and scientific papers

Synthesis and structure of diastereomers of pentenocin B produced by Trichoderma hamatum FO-6903

Ohira, Susumu,Fujiwara, Hiroyuki,Maeda, Kiyomi,Habara, Masaharu,Sakaedani, Naomi,Akiyama, Megumi,Kuboki, Atsuhito

, p. 1639 - 1641 (2007/10/03)

All diastereomers of pentenocin B, an inhibitor of interleukin-1β converting enzyme produced by Trichoderma hamatum FO-6903, were synthesized in chiral forms starting from L-threonine. Absolute configurations of natural pentenocin B were clarified to be 4S, 5R, and 6R.

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