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Benzene, 1-(1-butenyl)-4-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

658709-75-2

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658709-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 658709-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,8,7,0 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 658709-75:
(8*6)+(7*5)+(6*8)+(5*7)+(4*0)+(3*9)+(2*7)+(1*5)=212
212 % 10 = 2
So 658709-75-2 is a valid CAS Registry Number.

658709-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-but-1-enyl-4-nitrobenzene

1.2 Other means of identification

Product number -
Other names Benzene,1-(1-butenyl)-4-nitro

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:658709-75-2 SDS

658709-75-2Downstream Products

658709-75-2Relevant academic research and scientific papers

Rapid selective defunctionalization of the carbonyl group of α,β-unsaturated ketones with trialkoxylsilane/ZnX2

Li, Jiayun,Peng, Jiajian,Bai, Ying,Chen, Lingzhen,Lai, Guoqiao

scheme or table, p. 1621 - 1625 (2011/10/04)

Reduction of the carbonyl group of ketones to a methylene unit is widely applied in organic syntheses. In this article, we report that trialkoxylsilane/Zn-based catalyst systems may be applied in the reduction of the carbonyl groups of α,β-unsaturated ketones to methylene units under very mild conditions. In comparison with other Zn-based catalysts, excellent rates and high conversions of,-unsaturated ketones to methylene units are obtained using trialkoxylsilane/ZnI2 or ZnCl2. And the same time, the hydrosilylation reaction product could only be detected when using CuI, CuCl, or FeCl3. No reaction could be conducted by using trialkoxylsilane/CoCl2 or NiCl2, in comparison with Zn-based catalysts. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. Copyright Taylor &Francis Group, LLC.

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