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7237-52-7

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  • 6,9-Methano-5H-pyrido[1',2':1,2]azepino[4,5-b]indole-6(6aH)-carboxylicacid, 7-ethyl-7,8,9,10,12,13-hexahydro-, methyl ester, hydrochloride (1:1),(6S,6aS,7S,9R,11S)-

    Cas No: 7237-52-7

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  • Henan Tianfu Chemical Co., Ltd.
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7237-52-7 Usage

Description

[(Chlorogermanediyl)dimethanetriyl]tetrakis(trimethylsilane) is a chemical compound featuring a chlorogermanium center encircled by four trimethylsilyl groups. It is a highly reactive and versatile organometallic compound, known for its unique structure and reactivity, making it a valuable tool in the field of organometallic chemistry.

Uses

Used in Organic Synthesis:
[(Chlorogermanediyl)dimethanetriyl]tetrakis(trimethylsilane) is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions and form a wide range of products.
Used in Semiconductor Industry:
In the semiconductor industry, [(chlorogermanediyl)dimethanetriyl]tetrakis(trimethylsilane) is used as a material in the production of electronic components due to its unique properties.
Used as a Coating Agent:
[(Chlorogermanediyl)dimethanetriyl]tetrakis(trimethylsilane) is used as a coating agent for glass and ceramics, providing a protective layer and enhancing their properties.
Used in Polymer and Plastics Production:
[(chlorogermanediyl)dimethanetriyl]tetrakis(trimethylsilane) is also used in the production of polymers and plastics, where its reactivity and organometallic nature contribute to the development of new materials with specific characteristics.
Used in Organometallic Chemistry:
As an important precursor for the synthesis of other germanium-containing compounds, [(chlorogermanediyl)dimethanetriyl]tetrakis(trimethylsilane) is used in organometallic chemistry to create a variety of complex molecules with potential applications in various fields.
Safety Precaution:
It is crucial to handle [(chlorogermanediyl)dimethanetriyl]tetrakis(trimethylsilane) with caution, as it can react violently with water and air, which may pose risks to both the user and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 7237-52-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,3 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7237-52:
(6*7)+(5*2)+(4*3)+(3*7)+(2*5)+(1*2)=97
97 % 10 = 7
So 7237-52-7 is a valid CAS Registry Number.

7237-52-7SDS

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 [[bis(trimethylsilyl)methyl-chlorogermyl]-trimethylsilylmethyl]-trimethylsilane

1.2 Other means of identification

Product number -
Other names -

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:7237-52-7 SDS

7237-52-7Downstream Products

7237-52-7Relevant articles and documents

Synthesis of (-)-pseudotabersonine, (-)-pseudovincadifformine, and (+)-coronaridine enabled by photoredox catalysis in flow

Beatty, Joel W.,Stephenson, Corey R. J.

, p. 10270 - 10273 (2014/08/05)

Natural product modification with photoredox catalysis allows for mild, chemoselective access to a wide array of related structures in complex areas of chemical space, providing the possibility for novel structural motifs as well as useful quantities of less abundant congeners. While amine additives have been used extensively as stoichiometric electron donors for photocatalysis, the controlled modification of amine substrates through single-electron oxidation is ideal for the synthesis and modification of alkaloids. Here, we report the conversion of the amine (+)-catharanthine into the natural products (-)-pseudotabersonine, (-)-pseudovincadifformine, and (+)-coronaridine utilizing visible light photoredox catalysis.

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