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Benzenemethanamine, N,N-dimethyl-2-(phenyltelluro)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 157067-91-9 Structure
  • Basic information

    1. Product Name: Benzenemethanamine, N,N-dimethyl-2-(phenyltelluro)-
    2. Synonyms:
    3. CAS NO:157067-91-9
    4. Molecular Formula: C15H17NTe
    5. Molecular Weight: 338.907
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 157067-91-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzenemethanamine, N,N-dimethyl-2-(phenyltelluro)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenemethanamine, N,N-dimethyl-2-(phenyltelluro)-(157067-91-9)
    11. EPA Substance Registry System: Benzenemethanamine, N,N-dimethyl-2-(phenyltelluro)-(157067-91-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 157067-91-9(Hazardous Substances Data)

157067-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 157067-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,0,6 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 157067-91:
(8*1)+(7*5)+(6*7)+(5*0)+(4*6)+(3*7)+(2*9)+(1*1)=149
149 % 10 = 9
So 157067-91-9 is a valid CAS Registry Number.

157067-91-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-1-(2-phenyltellanylphenyl)methanamine

1.2 Other means of identification

Product number -
Other names 2-(N,N-dimethylaminomethyl)-1-phenyltellurobenzene

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:157067-91-9 SDS

157067-91-9Relevant articles and documents

Synthesis of intramolecularly coordinated heteroleptic diorganotellurides and diorganotelluroxides: Isolation of monomeric diorganotelluroxide [{2,6-(Me2NCH2)2C6H3}2TeO]and diorganohydroxyt

Gupta, Anand,Deka, Rajesh,Raju, Saravanan,Singh, Harkesh B.,Butcher, Ray J.

, p. 10 - 17 (2019)

A series of heteroleptic diorganotellurides (2-NMe2CH2C6H4)(R)Te, where R = C6H5 (5), 2-MeC6H4 (6), 2,6-MeC6H3 (7)and 2,6-iPrC6/

Immunoassay element containing a diaryl telluride compound to increase its stability

-

Page 10, (2010/02/03)

A dry immunoassay analytical element for assaying a ligand, comprising a support bearing: 1. an enzyme labeled ligand or an enzyme labeled receptor zone; 2. a spreading zone; and 3. a receptor zone containing a fixed concentration of an immobilized recept

Orthotellurated Derivatives of N,N-Dimethylbenzylamine: Crystal and Molecular Structures of tellurium(IV) Tribromide and dimethylammonium Chloride

Singh, Harkesh B.,Sudha, Narsimhan,West, Antony A.,Hamor, Thomas A.

, p. 907 - 913 (2007/10/02)

The reaction of o-lithiobenzylamine with elemental tellurium followed by air oxidation furnished an ill defined 'tellurinic anhydride'.Halogenolysis reactions of this with bromine and sulphonyl chloride afforded the corresponding trihalogenotellurium(IV) derivatives.Reduction of the trihalides with excess of hydrazine hydrate gave novel halogenotellurium(II) derivatives.Metathesis of the chlorotellurium(IV) and -(II) derivatives with sodium diethyldithiocarbamate resulted in the formation of dithiocarbamato derivatives.The crystal structure of tellurium(IV) tribromide is monoclinic, space group P21/n with a = 9.226(6), b = 15.439(8), c = 9.618(5) Angstroem, β = 94.94(5) deg, Z = 4, and R = 0.0419 for 938 observed reflections.The co-ordination about Te approximates to octahedral with a vacant equatorial site: two Br atoms axial, the third Br and the organic ligand equatorial (ax) 2.758(2) and 2.633(3), Te-Br(eq) 2.632(2), Te-C 2.12(1), and Te-N 2.42(1) Angstroem>.The compound is essentially monomeric, with a weak association between Te and a neighbouring bromine atom . dimethylammonium chloride is monoclinic, space group P21/n with a = 14.278(12), b= 8.349(5), c = 14.480(8) Angstroem, β = 93.59(5) deg, Z = 4, and R = 0.0288, for 2245 observed reflections.The co-ordination about Te can also be considered as octahedral with a vacant equatorial site: two chlorines apical, and the chloride ion and two carbon atoms equatorial .The quaternary nitrogen atom is twistedaway from the tellurium atom, Te...N 4.380(4) Angstroem, forming a hydrogen bond with a chloride ion.

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