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612-23-7

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612-23-7 Usage

Chemical Properties

liquid

Uses

Different sources of media describe the Uses of 612-23-7 differently. You can refer to the following data:
1. 2-Nitrobenzyl chloride has been used to introduce the photo labile 2-nitrobenzyl protecting group for the phenolic OH group of tyrosine. It is used as a pharmaceutical intermediate.
2. 2-Nitrobenzyl chloride was used in the synthesis of S-(2-nitrobenzyl)cysteine which was inserted into human erythropoietin. 2-Nitrobenzyl chloride was used to prepare 4,4′-dinitrostillbene.

General Description

Pale yellow crystals. Insoluble in water. Is thermally unstable.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

A halogenated aromatic nitro compound. Aromatic nitro compounds range from slight to strong oxidizing agents. If mixed with reducing agents, including hydrides, sulfides and nitrides, they may begin a vigorous reaction that culminates in a detonation. The aromatic nitro compounds may explode in the presence of a base such as sodium hydroxide or potassium hydroxide even in the presence of water or organic solvents. The explosive tendencies of aromatic nitro compounds are increased by the presence of multiple nitro groups.

Health Hazard

ACUTE/CHRONIC HAZARDS: Toxic. Lachrymator. Causes irritation on contact. Hazardous decomposition products. Mutagen.

Fire Hazard

2-NITROBENZYL CHLORIDE is combustible.

Biochem/physiol Actions

2-Nitrobenzyl chloride reacts with N-methyldiethanolamine and further reaction of the resulting quaternary diol with thionyl chloride at room temperature yields nitrobenzyl mustard quaternary salts.

Check Digit Verification of cas no

The CAS Registry Mumber 612-23-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 612-23:
(5*6)+(4*1)+(3*2)+(2*2)+(1*3)=47
47 % 10 = 7
So 612-23-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClNO2/c8-5-6-3-1-2-4-7(6)9(10)11/h1-4H,5H2

612-23-7 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (L13599)  2-Nitrobenzyl chloride, 98+%   

  • 612-23-7

  • 5g

  • 644.0CNY

  • Detail
  • Alfa Aesar

  • (L13599)  2-Nitrobenzyl chloride, 98+%   

  • 612-23-7

  • 25g

  • 2654.0CNY

  • Detail
  • Aldrich

  • (107336)  2-Nitrobenzylchloride  99%

  • 612-23-7

  • 107336-10G

  • 1,310.40CNY

  • Detail

612-23-7SDS

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 2-NITROBENZYL CHLORIDE

1.2 Other means of identification

Product number -
Other names 2-Nitrobenzyl chloride

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:612-23-7 SDS

612-23-7Relevant articles and documents

Bambusurils Bearing Nitro Groups and Their Further Modifications

Yawer, Mirza Arfan,Sleziakova, Kristina,Pavlovec, Lukas,Sindelar, Vladimir

, p. 41 - 47 (2018/01/17)

Bambusurils are recently developed neutral anion receptors that show a high affinity towards many inorganic anions, not only in organic solvents but also in water. However, the number of water-soluble bambusurils and also those bearing functional groups is very limited. In this paper we report the synthesis of four- and six-membered bambusurils containing eight and twelve nitro groups. All the nitro groups on the bambusuril portals could be transformed into amino functions, which provided the macrocycles with water solubility and allowed their further modification. For example, we have demonstrated the conversion of amino groups on the bambusurils into the corresponding urea-functionalized bambusuril derivatives. We also report the first example of a bambusuril bearing only two functional groups, which was prepared by the condensation of two different glycolurils.

Ortho-nitro benzyl chloride by a synthetic method of preparing pyraclostrobin intermediate (by machine translation)

-

Paragraph 0042, (2016/10/31)

This invention relates to a kind of the ortho-nitro benzyl chloride preparation pyraclostrobin method for synthesizing intermediate, comprising the following steps: in the ortho-nitro toluene, a catalyst is added, heating and stirring, and slowly inject chlorine, after the end of reaction, recovering O-nitro-toluene, ortho-nitro benzyl chloride obtained; the ortho-nitro benzyl chloride and 1 the [...] (the 4 [...] chlorolphenyl) - 3 the the pyrazole is mellow[...] for etherification reaction, to obtain the 2 [...] [(N -4 the [...] chlorolphenyl) - 3 the pyrazole oxygen radical[...] methyl] nitrobenzene. In this invention to replace nitryl chlorine animal pennitryl bromination animal pen and adjacent to the 1 [...] (the 4 [...] chlorolphenyl) - 3 the reaction the pyrazole is mellow[...], pyraclostrobin intermediates prepared by the 2 [...] [(N -4 the [...] chlorolphenyl) - 3 the pyrazole oxygen radical[...] methyl] nitrobenzene, avoid the use of a defect method for synthesis of O- nitryl bromination animal pen, content can be used for preparing ≥ 98%, yield ≥ 90% ether product. (by machine translation)

4-Aminophenyldiphenylphosphinite (APDPP), a new heterogeneous and acid scavenger phosphinite - Conversion of alcohols, trimethylsilyl, and tetrahydropyranyl ethers to alkyl halides with halogens or N-halosuccinimides

Iranpoor, Nasser,Firouzabadi, Habib,Gholinejad, Mohammad

, p. 1006 - 1012 (2007/10/03)

A new heterogeneous phosphinite, 4-aminophenyldiphenylphosphinite (APDPP), is prepared and used for the efficient conversion of alcohols, trimethylsilyl ethers, and tetrahydropyranyl ethers to their corresponding bromides, iodides, and chlorides in the presence of molecular halogens or N-halosuccinimides. The amino group in this phosphinite acts as an acid scavenger and removes the produced acid. A simple filtration easily removes the phosphinate by-product.

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