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998-39-0

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998-39-0 Usage

Chemical Properties

Different sources of media describe the Chemical Properties of 998-39-0 differently. You can refer to the following data:
1. clear colorless liquid
2. Reduces acid chlorides to aldehydes in presence of Pd(0). Effects free-radical reductive addition of alkyl halides to olefins. Reduces benzylic chlorides 70x faster than silyl hydrides.

Uses

Different sources of media describe the Uses of 998-39-0 differently. You can refer to the following data:
1. Efficient reducing agent for benzylic chlorides.1
2. Tri-n-butylgermanium hydride is used in the reduction of benzylic chlorides. It is also used as pharmaceutical intermediate.

General Description

Tributylgermanium hydride is a radical generating reagent. Reductive alkylation of active olefins with alkyl halides with tributylgermanium hydride was investigated in detail.

Check Digit Verification of cas no

The CAS Registry Mumber 998-39-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,9 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 998-39:
(5*9)+(4*9)+(3*8)+(2*3)+(1*9)=120
120 % 10 = 0
So 998-39-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H27Ge/c1-4-7-10-13(11-8-5-2)12-9-6-3/h4-12H2,1-3H3

998-39-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (42688)  Tri-n-butylgermanium hydride, 97+%   

  • 998-39-0

  • 1g

  • 665.0CNY

  • Detail
  • Alfa Aesar

  • (42688)  Tri-n-butylgermanium hydride, 97+%   

  • 998-39-0

  • 5g

  • 3029.0CNY

  • Detail
  • Aldrich

  • (409170)  Tributylgermaniumhydride  99%

  • 998-39-0

  • 409170-1G

  • 1,932.84CNY

  • Detail

998-39-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tributylgermane

1.2 Other means of identification

Product number -
Other names Tri-n-butylgermanium hydride

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:998-39-0 SDS

998-39-0Relevant articles and documents

Photodecompostion of the Oligogermanes nBu3GeGePh2GenBu3 and nBu3GeGePh3: Identification of the Photoproducts by Spectroscopic and Spectrometric Methods

Komanduri, Sangeetha P.,Schrick, Aaron C.,Feasley, Christa L.,Dufresne, Craig P.,Weinert, Charles S.

, p. 3196 - 3203 (2016/07/14)

The oligogermane nBu3GeGePh2GenBu3was photolyzed using UV-C light in the presence of acetic acid as a trapping agent and the photoproducts were identified using1H NMR spectroscopy, gas chromatography/electron-impact mass spectrometry, and high resolution accurate mass mass spectrometry. The products identified were the germanes nBu3GeH, nBu3GeOAc, and Ph2Ge(H)OAc (OAc = C2H3O2) and the digermane nBu6Ge2. This indicates that both germanium–germanium single bonds are cleaved homolytically upon irradiation to generate two nBu3Ge·radicals and the germylene Ph2Ge:. The digermane nBu3GeGePh3was also photolyzed under identical conditions, and in this case the photoproducts were identified as nBu3GeH, nBu3GeOAc, Ph3GeH, Ph3GeOAc and the digermanes nBu6Ge2and Ph6Ge2.

Cp2TiCl2 catalyzed one-pot synthesis of n-Bu3GeH from GeCl4

Colacot, Thomas J.

, p. 378 - 381 (2007/10/03)

The reaction of GeCl4 with n-BuMgCl in presence of a catalytic amount of Cp2TiCl2 gives n-Bu3GeH and n-Bu4Ge in ca. 70 and 25% yield, respectively. This method provides an industrially feasible one-pot synthesis for Bu3GeH and Bu4Ge. The reaction temperature and stoichiometry seem to be important in the distribution of the products. Apart from elemental analysis these compounds have been characterized by comparing their boiling points, NMR spectral data and GC assay with that of the authentic samples.

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