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Germane, tributyl(2-phenylethenyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38796-01-9

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38796-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38796-01-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,9 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38796-01:
(7*3)+(6*8)+(5*7)+(4*9)+(3*6)+(2*0)+(1*1)=159
159 % 10 = 9
So 38796-01-9 is a valid CAS Registry Number.

38796-01-9SDS

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 (E)-1-phenyl-2-(tri-n-butylgermyl)ethylene

1.2 Other means of identification

Product number -
Other names (E)-β-tri-n-butylgermylstyrene

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:38796-01-9 SDS

38796-01-9Downstream Products

38796-01-9Relevant academic research and scientific papers

Cobalt-Catalyzed (E)-β-Selective Hydrogermylation of Terminal Alkynes

Radzhabov, Maxim R.,Mankad, Neal P.

supporting information, p. 3221 - 3226 (2021/05/04)

A cobalt-catalyzed method for the hydrogermylation of alkynes is reported, providing a selective and accessible route to (E)-β-vinyl(trialkyl)germanes from terminal alkynes and HGeBu3. As shown in multiple examples, the developed method demonstrates a broad functional group tolerance an practical utility for late-stage hydrogermylation of natural products. The method is compatible with alkynes bearing both aryl and alkyl substituents, providing unrivaled selectivity for previously challenging 1° alkyl-substituted alkynes. Moreover, the catalyst used in this method, Co2(CO)8, is a cheap and commercially available reagent. Conducted mechanistic studies supported the syn-addition of Bu3GeH to an alkyne π-complex.

Transition metal-catalyzed dehydrogenative germylation of olefins with tri-n-butylgermane

Furukawa, Naoyuki,Kourogi, Noriko,Seki, Yoshio,Kakiuchi, Fumitoshi,Murai, Shinji

, p. 3764 - 3767 (2008/10/08)

The catalyzed reaction of an excess of styrene with n-Bu3GeH using several ruthenium and rhodium complexes gave the corresponding vinylgermanes (α-trin-butylgermylstyrene, (Z)-β-tri-n-butylgermylstyrene, and (E)-β-tri-n-butylgermylstyrene), whi

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