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1529-48-2

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1529-48-2 Usage

Chemical Properties

clear colorless liquid

Uses

Dimethylgermanium dichloride is a useful organogermanium compound for synthesis and proteomics research. It is also used as an organic intermediate and in chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 1529-48-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,2 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1529-48:
(6*1)+(5*5)+(4*2)+(3*9)+(2*4)+(1*8)=82
82 % 10 = 2
So 1529-48-2 is a valid CAS Registry Number.
InChI:InChI=1/C2H6Ge.2ClH/c1-3-2;;/h1-2H3;2*1H/q+2;;/p-2

1529-48-2 Well-known Company Product Price

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  • Alfa Aesar

  • (34107)  Dimethylgermanium dichloride, 98+%   

  • 1529-48-2

  • 0.5g

  • 202.0CNY

  • Detail
  • Alfa Aesar

  • (34107)  Dimethylgermanium dichloride, 98+%   

  • 1529-48-2

  • 2g

  • 699.0CNY

  • Detail
  • Alfa Aesar

  • (34107)  Dimethylgermanium dichloride, 98+%   

  • 1529-48-2

  • 10g

  • 3291.0CNY

  • Detail
  • Aldrich

  • (336785)  Dimethylgermaniumdichloride  99%

  • 1529-48-2

  • 336785-1G

  • 423.54CNY

  • Detail

1529-48-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name DIMETHYLGERMANIUM DICHLORIDE

1.2 Other means of identification

Product number -
Other names Dimethylgermanium dichloride

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:1529-48-2 SDS

1529-48-2Relevant articles and documents

Organometallic compounds of the lanthanides. 64. Synthesis and X-ray crystal structures of dimethylgermyl bis(tetramethylcyclopentadienyl) halide and alkyl derivatives of the lanthanides

Schumann, Herbert,Esser, Lothar,Loebel, J?rg,Dietrich, Andreas,Van Der Helm, Dick,Ji, Xinhua

, p. 2585 - 2592 (1991)

Metathesis of Me2GeCl2 or Me2SnCl2 with 2 equiv of LiC5Me4H affords Me2Ge(C5Me4H)2 (1) and Me2Sn(C5Me4H)2 (2), respectively. The subsequent deprotonation of 1 with MeLi yields only the desired dilithium salt Me2Ge(C5Me4Li)2 (3) whereas 2 forms Me4Sn and two LiC5Me4H. The trichlorides of neodymium, samarium, holmium, and lutetium react with the dilithium salt 3 with the formation of Me2Ge(C5Me4)2LnCl 2Li(THF)2 (Ln = Nd (4), Sm (5), Ho (6), Lu (7)). The reaction of 4 and 6 with LiCH(SiMe3)2 produces Me2Ge(C5Me4)2LnCH(SiMe 3)2 (Ln = Nd (8), Ho (9)). The new compounds have been characterized by elemental analysis, mass and NMR spectra, as well as X-ray structural analysis of 5, 7, and 9. The halides 5 and 7 crystallize in the monoclinic space group P21/c (No. 14) with a = 9.7284 (9), b = 19.397 (1), c = 16.610 (2) ?, β = 98.963 (9)°; Z = 4 or a = 9.578 (3), b = 19.218 (4), c = 16.525 (4) ?, β = 99.73 (2)°; Z = 4, respectively. Least-squares refinement led to a final R value of 0.020 (Fo > 4σ(Fo)) for 5554 independent reflections for 5 or of 0.028 (Fo > 3σ(Fo)) for 5822 independent reflections for 7. Compound 9 crystallizes in the monoclinic space group P21/m (No. 11) with a = 9.2621 (8), b = 14.216 (2), c = 11.839 (2) ?, β = 107.79 (1)°, Z = 2, and R = 0.023 (Fo > 4σ(Fo)) for 2954 reflections. The structure of 9 shows a short Ho-C (methyl) contact of 2.774 (4) ?.

Molecular Oligogermanes and Related Compounds: Structure, Optical and Semiconductor Properties

Zaitsev, Kirill V.,Tafeenko, Viktor A.,Oprunenko, Yuri F.,Kharcheva, Anastasia V.,Zhanabil, Zhaisan,Suleimen, Yerlan,Lam, Kevin,Zaitsev, Vladimir B.,Zaitseva, Anna V.,Zaitseva, Galina S.,Karlov, Sergey S.

, p. 1240 - 1249 (2017)

The optical (UV/Vis absorbance, fluorescence in the solid state and in solution) and semiconducting properties of a number of di- and trigermanes as well as related silicon- and tin-containing germanes, 1–6 ((p-Tol)3GeGeMe3 (1), Ph3SnGe(SiMe3)3 (2), (C6F5)3GeGePh3 (3), (p-Tol)3GeSiMe2SiMe3 (4), (p-Tol)3GeGeMe2Ge(p-Tol)3 (5), (p-Tol)3GeSiMe2SiMe2Ge(p-Tol)3 (6)) were investigated. Molecular structures of 5 and 6 were studied by X-ray diffraction analysis. All compounds displayed luminescence properties. In addition, a band gap (of about 3.3 eV) was measured for compounds 1–6 showing that those molecules display semiconductor properties.

Transient and Matrix Ultraviolet Absorption Spectra of Dimethylgermylene (Dimethylgermanediyl)

Tomoda, Shuji,Shimoda, Masakatsu,Takeuchi, Yoshito,Kajii, Yoshizumi,Obi, Kinichi,et al.

, p. 910 - 912 (1988)

Dimethylgermylene (1), generated from a new precursor dimethylbis(phenylseleno)germane (2), has been observed as a transient species by time-resolved laser flash photolysis at room temperature.

Wieber et al.

, p. 79,81, 82 (1967)

Belij et al.

, p. 485 (1969)

Fast kinetic studies of the reactivities of transient germylenes in methanol and tetrahydrofuran solution

Lollmahomed, Farahnaz,Huck, Lawrence A.,Harrington, Cameron R.,Chitnis, Saurabh S.,Leigh, William J.

, p. 1484 - 1494 (2009/07/18)

Laser flash photolysis techniques have been employed to study the reactivities of dimethylgermylene (GeMe2), diphenylgermylene (GePh2), and a series of ring-substituted diarylgermylenes (GeAr 2) in methanol (MeOH) and tetr

Studies of photochemical reactions of 7,8-digermabicyclo[2.2.2]octadienes by steady-state and laser flash photolysis techniques

Mochida, Kunio,Kayamori, Takanari,Wakasa, Masanobu,Hayashi, Hisaharu,Egorov, Mikhail P.

, p. 3379 - 3386 (2008/10/08)

The photochemistry of 1,4-diphenyl-2,3-benzo-7,7,8,8-tetraalkyl-7, 8-digermabicyclo[2.2.2]-octadienes in solution has been studied in detail by steady-state, nanosecond laser flash photolysis, and matrix isolation techniques. Photolysis of 7,8-digermabicy

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