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116246-83-4

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116246-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116246-83-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,2,4 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 116246-83:
(8*1)+(7*1)+(6*6)+(5*2)+(4*4)+(3*6)+(2*8)+(1*3)=114
114 % 10 = 4
So 116246-83-4 is a valid CAS Registry Number.

116246-83-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethoxycarbonylmethyl phenyl telluride

1.2 Other means of identification

Product number -
Other names .ethyl-α-phenyltelluro acetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:116246-83-4 SDS

116246-83-4Relevant articles and documents

Substituent Effects and Stereochemistry in 125Te NMR Spectroscopy. Diorganyltellurium Dihalides and Some Tellurides and Ditellurides

Duddeck, Helmut,Biallass, Armin

, p. 303 - 311 (2007/10/02)

125Te, 19F and 13C NMR data for 33 compounds containing tellurium substituents are presented.The 125Te chemical shifts in (PhTeCl2)R compounds are between δ=878 and 1023; in corresponding (PhTeF2)R compounds they are 220 to 360 ppm larger.Effects of subst

Synthesis and 125Te NMR spectroscopy of α-tellurocarbonyl compounds and derivatives

Silks III,Odom,Dunlap

, p. 1105 - 1119 (2007/10/02)

The reaction of lithium alkyl-, alkenyl-, alkynyl-, and aryl tellurolates with α-bromocarbonyl compounds in anhydrous tetrahydrofuran gives the title compounds in yields ranging from 55-92%. The 125Te NMR chemical shift range for these compound

Synthesis of α-Phenyltelluro Carbonyl Compounds

Hiiro, Tomoki,Kambe, Nobuaki,Ogawa, Akiya,Miyoshi, Noritaka,Murai, Shinji,Sonoda, Noboru

, p. 1096 - 1097 (2007/10/02)

Several new α-phenyltelluro carbonyl compounds have been synthesized by the reaction of benzenetellurenyl iodide with lithium enolates derived from ketones, esters, and an amide in tetrahydrofuran at -78 deg C.

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