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Benzenethiolate, also known as phenyl mercaptan, is an organic compound with the chemical formula C6H5SH. It is a colorless liquid with a strong, unpleasant odor and is used as a reagent in organic synthesis, particularly in the preparation of various sulfur-containing compounds. Trimethylgermanium, on the other hand, is an organogermanium compound with the chemical formula (CH3)3Ge. It is a colorless, volatile liquid that is sensitive to air and moisture. Trimethylgermanium is primarily used as a precursor in the synthesis of various organogermanium compounds and as a dopant in semiconductor materials. Both benzenethiolate and trimethylgermanium are hazardous chemicals and require proper handling and storage to prevent exposure and environmental contamination.

4848-62-8

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4848-62-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4848-62-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,4 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4848-62:
(6*4)+(5*8)+(4*4)+(3*8)+(2*6)+(1*2)=118
118 % 10 = 8
So 4848-62-8 is a valid CAS Registry Number.

4848-62-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl(phenylsulfanyl)germane

1.2 Other means of identification

Product number -
Other names Germane,trimethyl(phenylthio)

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:4848-62-8 SDS

4848-62-8Relevant academic research and scientific papers

Thioether complexes of tungsten hexacarbonyl

Lucas, C. Robert

, p. 1758 - 1763 (2007/10/02)

The preparation of a series of organic and organometallic thioethers R3MSR' (M = C,Si,Ge, or Sn) is reported.From these, several new compounds of type 1 are synthesized, some of which contain para-substituted aryl functions for R and R'.In hexane solution in the carbonyl streching region of the ir the uv there is evidence for a degree of multiple bonding, at least in the M - S - WW - CO portion of these molecules.Multiple bonding extending into aromatic R or R'is small or non-existent and cannot be assessed precisely because of spontaneous decomposition of the complexes.All the complexes undergo a thermally initiated decomposition, the case of which depends on the nature of R, R', and M.The unusual W(I) thiolate cis-2 is the termal decomposition product.

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