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199285-79-5

2-Naphthalenemethanol, a-(nitromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 199285-79-5 Structure

  • Basic information

    1. Product Name: 2-Naphthalenemethanol, a-(nitromethyl)-
    2. Synonyms:
    3. CAS NO:199285-79-5
    4. Molecular Formula: C12H11NO3
    5. Molecular Weight: 217.224
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 199285-79-5.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: 2-Naphthalenemethanol, a-(nitromethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Naphthalenemethanol, a-(nitromethyl)-(199285-79-5)
    11. EPA Substance Registry System: 2-Naphthalenemethanol, a-(nitromethyl)-(199285-79-5)

  • 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: 199285-79-5(Hazardous Substances Data)

199285-79-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 199285-79-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,2,8 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 199285-79:
(8*1)+(7*9)+(6*9)+(5*2)+(4*8)+(3*5)+(2*7)+(1*9)=205
205 % 10 = 5
So 199285-79-5 is a valid CAS Registry Number.

199285-79-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(naphthalen-2-yl)-2-nitroethanol

1.2 Other means of identification

Product number -
Other names 1-(naphthalen-6-yl)-2-nitroethanol

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:199285-79-5 SDS

199285-79-5Relevant articles and documents

Investigation of DNA as a catalyst for Henry reaction in water

Fan, Jinmin,Sun, Gaojun,Wan, Changfeng,Wang, Zhiyong,Li, Yingfu

, p. 3792 - 3794 (2008)

Double-stranded DNA of natural origin can be used to facilitate nitro-aldol (or Henry) reaction in aqueous solution. The Royal Society of Chemistry.

Direct Henry reactions with modified calcium oxide as solid catalyst

Tang, Ying,Gu, Xuefan,Meng, Mei,Xu, Jingfang

, p. 3715 - 3725 (2013/10/22)

Commercial CaO was modified simply with benzyl bromide. The modified CaO had good water resistance, and characterization by FTIR and TG revealed the modifier was chemically bonded to the CaO surface. Commercial CaO and CaO modified with benzyl bromide were investigated as catalysts for the Henry reaction between benzaldehyde and nitromethane. It was found that the catalytic activity of the modified CaO was greatly improved, with high conversion of benzaldehyde to the (E)-phenyl nitroolefin and 1-phenyl-2-nitroethanol, and with different selectivity from commercial CaO. The effect of modification and reaction conditions on yield, selectivity, and mechanism were studied thoroughly.

One-pot synthesis of nitroalkenes via the Henry reaction over amino-functionalized MIL-101 catalysts

Yu, Huixian,Xie, Jianwu,Zhong, Yijun,Zhang, Fumin,Zhu, Weidong

, p. 101 - 104 (2013/01/15)

Ethylenediamine moieties with different amounts were incorporated into the metal-organic framework MIL-101 to prepare the amino-functionalized MIL-101 materials, which were used as heterogeneous catalysts in the one-pot synthesis of nitroalkenes via the Henry reaction. Various reaction conditions were optimized. Under the optimized conditions, the selectivity towards nitroalkenes is extremely high in combination with nearly complete conversion of the reactant nitroalkanes. The amino-functionalized MIL-101 behaves as a true heterogeneous catalyst, can be easily recovered by filtration, and can be reused at least twice without significant loss of its catalytic performance.

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