Cas 773872-99-4,[2-(3-thienyl)phenyl]methanol

773872-99-4

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Basic information

Product Name: [2-(3-thienyl)phenyl]methanol
Synonyms:
CAS NO:773872-99-4
Molecular Formula:
Molecular Weight: 190.266
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: [2-(3-thienyl)phenyl]methanol(CAS DataBase Reference)
NIST Chemistry Reference: [2-(3-thienyl)phenyl]methanol(773872-99-4)
EPA Substance Registry System: [2-(3-thienyl)phenyl]methanol(773872-99-4)

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: 773872-99-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 773872-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,3,8,7 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 773872-99:
(8*7)+(7*7)+(6*3)+(5*8)+(4*7)+(3*2)+(2*9)+(1*9)=224
224 % 10 = 4
So 773872-99-4 is a valid CAS Registry Number.

773872-99-4Upstream product

773872-99-4Downstream Products

773872-99-4Relevant academic research and scientific papers

Electrophilicity and nucleophilicity of commonly used aldehydes

Pratihar, Sanjay

, p. 5781 - 5788 (2014)

The present approach for determining the electrophilicity (E) and nucleophilicity (N) of aldehydes includes a kinetic study of KMNO4 oxidation and NaBH4 reduction of aldehydes. A transition state analysis of the KMNO4 promoted aldehyde oxidation reaction has been performed, which shows a very good correlation with experimental results. The validity of the experimental method has been tested using the experimental activation parameters of the two reactions. The utility of the present approach is further demonstrated by the theoretical versus experimental relationship, which provides easy access to E and N values for various aldehydes and offers an at-a-glance assessment of the chemical reactivity of aldehydes in various reactions. the Partner Organisations 2014.

A new synthetic approach to 6-unsubstituted phenanthridine and phenanthridine-like compounds under mild and metal-free conditions

Tummatorn, Jumreang,Krajangsri, Suppachai,Norseeda, Krissada,Thongsornkleeb, Charnsak,Ruchirawat, Somsak

, p. 5077 - 5081 (2014/07/08)

A new and mild synthetic approach for the synthesis of 6-unsubstituted phenanthridine and phenanthridine-like compounds under metal-free conditions at room temperature has been developed. The strategy involved a tandem azide rearrangement/intramolecular annulation and oxidation reactions of biarylmethyl azide precursors to obtain the desired products in up to 99% yields with high regioselectivity.

Photochemical generation of thiophene analogs of 9-fluorenyl cations

Bancerz, Mathew,Huck, Lawrence A.,Leigh, William J.,Mladenova, Gabriela,Najafian, Katayoun,Zeng, Xiaofeng,Lee-Ruff, Edward

experimental part, p. 1202 - 1213 (2011/09/12)

The 9-fluorenyl cation is a member of the 4N Hueckel antiaromatic series of intermediates, first observed by time-resolved spectroscopy on UV photo-excitation of 9-fluorenol. Thiophene analogs of 9-fluorenol in which one of the annelated benzene rings is

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