Cas 887307-88-2,(αS)-α-[1,1-dimethyl-2-[(S)-(4-methylphenyl)sulfinyl]-2-propenyl]-2-furanmethanol

887307-88-2

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Basic information

Product Name: (αS)-α-[1,1-dimethyl-2-[(S)-(4-methylphenyl)sulfinyl]-2-propenyl]-2-furanmethanol
Synonyms: (αS)-α-[1,1-dimethyl-2-[(S)-(4-methylphenyl)sulfinyl]-2-propenyl]-2-furanmethanol
CAS NO:887307-88-2
Molecular Formula:
Molecular Weight: 304.41
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: (αS)-α-[1,1-dimethyl-2-[(S)-(4-methylphenyl)sulfinyl]-2-propenyl]-2-furanmethanol(CAS DataBase Reference)
NIST Chemistry Reference: (αS)-α-[1,1-dimethyl-2-[(S)-(4-methylphenyl)sulfinyl]-2-propenyl]-2-furanmethanol(887307-88-2)
EPA Substance Registry System: (αS)-α-[1,1-dimethyl-2-[(S)-(4-methylphenyl)sulfinyl]-2-propenyl]-2-furanmethanol(887307-88-2)

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: 887307-88-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 887307-88-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,3,0 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 887307-88:
(8*8)+(7*8)+(6*7)+(5*3)+(4*0)+(3*7)+(2*8)+(1*8)=222
222 % 10 = 2
So 887307-88-2 is a valid CAS Registry Number.

887307-88-2Upstream product

887307-88-2Downstream Products

887307-88-2Relevant academic research and scientific papers

New multicomponent approach for the creation of chiral quaternary centers in the carbonyl allylation reactions

Sklute, Genia,Marek, Ilan

, p. 4642 - 4649 (2007/10/03)

The combined regio- and stereo-controlled carbometalation reaction of alkynyl sulfoxide followed by a zinc homologation and finally an allylation reaction led, in a single-pot operation, to chiral homoallylic alcohols in excellent yields and diastereosele

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