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1-(hex-5-en-1-yloxy)-4-nitrobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 108705-97-1 Structure
  • Basic information

    1. Product Name: 1-(hex-5-en-1-yloxy)-4-nitrobenzene
    2. Synonyms: 1-(hex-5-en-1-yloxy)-4-nitrobenzene
    3. CAS NO:108705-97-1
    4. Molecular Formula:
    5. Molecular Weight: 221.256
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 108705-97-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(hex-5-en-1-yloxy)-4-nitrobenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(hex-5-en-1-yloxy)-4-nitrobenzene(108705-97-1)
    11. EPA Substance Registry System: 1-(hex-5-en-1-yloxy)-4-nitrobenzene(108705-97-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 108705-97-1(Hazardous Substances Data)

108705-97-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108705-97-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,7,0 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 108705-97:
(8*1)+(7*0)+(6*8)+(5*7)+(4*0)+(3*5)+(2*9)+(1*7)=131
131 % 10 = 1
So 108705-97-1 is a valid CAS Registry Number.

108705-97-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(hex-5-enyloxy)-4-nitrobenzene

1.2 Other means of identification

Product number -
Other names 4-(hex-5-enyloxy)nitrobenzene

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:108705-97-1 SDS

108705-97-1Relevant articles and documents

Regioselective Metal-Free Aza-Heck Reactions of Terminal Alkenes Catalyzed by Phosphine Selenides

Zheng, Tianyi,Tabor, John R.,Stein, Zackary L.,Michael, Forrest E.

, p. 6975 - 6978 (2018/11/21)

Phosphine selenides are introduced as an alternate class of selenium-based catalysts for the aza-Heck reaction of alkenes. Using these catalysts, a range of terminal alkenes react with NFBS to give oxidative amination products. Judicious choice of phosphi

A novel design for porphyrin based D-s-A systems as molecular rectifiers

Garg, Kavita,Majumder, Chiranjib,Gupta, Shiv K.,Aswal, Dinesh Kumar,Nayak, Sandip Kumar,Chattopadhyay, Subrata

, p. 1548 - 1557 (2016/02/09)

Two Si-based hybrid self-assembled monolayers of porphyrin based on a D-s-A system were synthesized by electro-grafting. The monolayers showed a stable and reversible rectification at room temperature. The monolayer fabricated using a porphyrin with an eleven-carbon alkyl chain linker was comparatively more compact and exhibited a 105 times higher rectification ratio (RR) relative to another similar system that had a six-carbon alkyl chain linker, possibly because of the compact packing.

Radical chain reduction of alkylboron compounds with catechols

Villa, Giorgio,Povie, Guillaume,Renaud, Philippe

supporting information; experimental part, p. 5913 - 5920 (2011/06/16)

The conversion of alkylboranes to the corresponding alkanes is classically per-formed via protonolysis of alkylboranes. This simple reaction requires the use of severe reaction conditions, that is, treatment with a carboxylic acid at high temperature (>150 °C). We report here a mild radical procedure for the transformation of organoboranes to alkanes. 4-tert-Butylcatechol, a well-established radical inhibitor and antioxidant, is acting as a source of hydrogen atoms. An efficient chain reaction is observed due to the exceptional reactivity of phenoxyl radicals toward alkylboranes. The reaction has been applied to a wide range of organoboron derivatives such as B- alkylcatecholboranes, trialkylboranes, pinacolboronates, and alkylboronic acids. Furthermore, the so far elusive rate constants for the hydrogen transfer between secondary alkyl radical and catechol derivatives have been experimentally determined. Interestingly, they are less than 1 order of magnitude slower than that of tin hydride at 80 °C, making catechols particularly attractive for a wide range of transformations involving C-C bond formation.

Enzyme activity fingerprinting with substrate cocktails

Goddard, Jean-Philippe,Reymond, Jean-Louis

, p. 11116 - 11117 (2007/10/03)

In the postgenomic era, emphasis is shifting from protein identification to protein functional analysis. Enzyme function can be characterized by measuring activity across series of substrates, which generates an activity profile or fingerprint. Activity f

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