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695-64-7

Cyclohexane, 1-chloro-1-nitroso, also known as 1-chloro-1-nitrosocyclohexane, is an organic compound with the chemical formula C6H10ClNO. It is a derivative of cyclohexane, where one hydrogen atom is replaced by a chloro group and a nitroso group. Cyclohexane, 1-chloro-1-nitroso- is characterized by its cyclic structure, with six carbon atoms arranged in a ring, and the presence of a chlorine atom and a nitroso group attached to one of the carbon atoms. Cyclohexane, 1-chloro-1-nitroso, is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, and it is also used in the production of dyes and other specialty chemicals. Due to its reactive nature, it is essential to handle this compound with care, following proper safety protocols to minimize potential hazards.

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  • 695-64-7 Structure

  • Basic information

    1. Product Name: Cyclohexane, 1-chloro-1-nitroso-
    2. Synonyms: Cyclohexane, 1-chloro-1-nitroso-;α-chloronitrosocyclohexane;1-CHLORONITROSOCYCLOHEXANE
    3. CAS NO:695-64-7
    4. Molecular Formula: C6H10ClNO
    5. Molecular Weight: 147.6027
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 695-64-7.mol

  • Chemical Properties

    1. Melting Point: 116.5°C
    2. Boiling Point: 62-63 °C(Press: 22 Torr)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.1140
    6. Refractive Index: 1.4870 (estimate)
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Cyclohexane, 1-chloro-1-nitroso-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexane, 1-chloro-1-nitroso-(695-64-7)
    11. EPA Substance Registry System: Cyclohexane, 1-chloro-1-nitroso-(695-64-7)

  • Safety Data

    1. Hazard Codes:  3:;
    2. Statements: N/A
    3. Safety Statements: − and NOx." target="_blank">May explode during vacuum distillation. When heated to decomposition it emits toxic fumes of C
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 695-64-7(Hazardous Substances Data)

695-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 695-64-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 695-64:
(5*6)+(4*9)+(3*5)+(2*6)+(1*4)=97
97 % 10 = 7
So 695-64-7 is a valid CAS Registry Number.

695-64-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name α-chloronitrosocyclohexane

1.2 Other means of identification

Product number -
Other names 1-CHLORO-1-NITROSOCYCLOHEXANE

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:695-64-7 SDS

695-64-7Relevant articles and documents

New and improved methods for the conversion of nitroalkanes into geminal chloronitroso compounds

Bou-Moreno, Rafael,Luengo-Arratta, Sandra,Pons, Valerie,Motherwell, William B.

, p. 6 - 12 (2013/03/13)

The scope and limitations of a new method for the preparation of geminal chloronitroso compounds involving treatment of a nitronate anion with oxalyl chloride are described in full, and a milder, high yielding, and more chemoselective variant using the de

Observations on the reaction of nitronate anions with oxalyl chloride: A new method for the preparation of geminal chloronitroso compounds

Bou-Moreno, Rafael,Luengo-Arratta, Sandra,Motherwell, William B.

supporting information; experimental part, p. 2097 - 2099 (2011/05/09)

A simple method for the preparation of geminal chloronitroso compounds from secondary nitro compounds via their derived nitronate anions is presented.

Generation of nitryl chloride from chlorotrimethylsilane-acetyl nitrate reaction: A one-pot preparation of gem-chloronitro compounds from oximes

Mohammed, Abdulkarim H. A.,Nagendrappa, Gopalpur

experimental part, p. 571 - 577 (2010/12/20)

While iso-amyl nitrite reacts with chlorotrimethylsilane to give NOCl, iso-amyl nitrate does not yield NO 2Cl with silicon reagent. However, acetyl nitrate reacts successfully with chlorotrimethylsilane to give nitryl chloride, which is charact

N,N′-Dichloro bis(2,4,6-trichlorophenyl)urea (CC-2): an efficient reagent for the synthesis of α-chloro-nitroso compounds

Gupta,Acharya,Pardasani,Dubey

, p. 767 - 770 (2007/10/03)

A simple, efficient, rapid, and mild method for the synthesis of α-chloro-nitroso compounds is described using bis(2,4,6-trichlorophenyl)urea (CC-2).

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