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2817-41-6

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2817-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2817-41-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,1 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2817-41:
(6*2)+(5*8)+(4*1)+(3*7)+(2*4)+(1*1)=86
86 % 10 = 6
So 2817-41-6 is a valid CAS Registry Number.

2817-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name triethyl(phenyl)germane

1.2 Other means of identification

Product number -
Other names Germane,triethylphenyl

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:2817-41-6 SDS

2817-41-6Relevant articles and documents

Germylation of Arenes via Pd(I) Dimer Enabled Sulfonium Salt Functionalization

Gevondian, Avetik G.,Schoenebeck, Franziska,Selmani, Aymane

, (2020/06/29)

While aryl germanes have recently found usage as coupling partners in powerful catalytic applications, the synthetic access to this promising functionality is currently limited. This report details the straightforward synthesis of functionalized aryl trie

General access to para-substituted styrenes

Langle, Sandrine,David-Quillot, Franck,Balland, Alexia,Abarbri, Mohamed,Duchêne, Alain

, p. 113 - 119 (2007/10/03)

A simple and efficient procedure has been developed for the synthesis of organogermanium compounds and styrenes para-substituted with groups containing an atom of the 14th group by one-pot reaction of halogenosilanes, germanes or stannanes, organic halides and magnesium using ultrasound methods.

Reactivities of triethylgermylborate in methanol

Nanjo, Masato,Matsudo, Kazuhiko,Mochida, Kunio

, p. 1086 - 1087 (2007/10/03)

The reactivity of lithium (triethylgermyl)triphenylborate, prepared from unsolvated triethylgermyllithium and triphenylborane, with organic substrates in methanol was investigated. The germylborates reacted with organic halides and acyl halides to give th

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