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1,3-DIISOPROPYLCYCLOHEXANE is a chemical compound characterized by a cyclohexane ring with two isopropyl groups attached at the 1 and 3 positions. It is a clear, colorless liquid with a slightly sweet odor, known for its low toxicity and minimal environmental impact. 1,3-DIISOPROPYLCYCLOHEXANE's stability under normal conditions and its non-highly reactive nature make it a versatile and reliable choice for various industrial applications.

7045-70-7

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7045-70-7 Usage

Uses

Used in Chemical Industry:
1,3-DIISOPROPYLCYCLOHEXANE is used as a solvent for its ability to dissolve a wide range of substances, making it suitable for use in the production of paints, coatings, and adhesives. Its properties contribute to the efficiency and performance of these products.
Used as an Intermediate in Chemical Production:
1,3-DIISOPROPYLCYCLOHEXANE serves as an intermediate in the synthesis of other chemicals, facilitating the creation of a variety of compounds for different applications across various industries. Its role in chemical synthesis is crucial for producing a range of end products.

Check Digit Verification of cas no

The CAS Registry Mumber 7045-70-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,4 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7045-70:
(6*7)+(5*0)+(4*4)+(3*5)+(2*7)+(1*0)=87
87 % 10 = 7
So 7045-70-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H24/c1-9(2)11-6-5-7-12(8-11)10(3)4/h9-12H,5-8H2,1-4H3

7045-70-7 Well-known Company Product Price

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  • Alfa Aesar

  • (B21390)  1,3-Diisopropylcyclohexane, cis + trans, 97+%   

  • 7045-70-7

  • 5g

  • 578.0CNY

  • Detail
  • Alfa Aesar

  • (B21390)  1,3-Diisopropylcyclohexane, cis + trans, 97+%   

  • 7045-70-7

  • 25g

  • 1838.0CNY

  • Detail

7045-70-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-di(propan-2-yl)cyclohexane

1.2 Other means of identification

Product number -
Other names 1,3-Diisopropyl-cyclohexan

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:7045-70-7 SDS

7045-70-7Downstream Products

7045-70-7Relevant academic research and scientific papers

Enantio- and Regioselective Ir-Catalyzed Hydrogenation of Di- and Trisubstituted Cycloalkenes

Peters, Byron K.,Liu, Jianguo,Margarita, Cristiana,Rabten, Wangchuk,Kerdphon, Sutthichat,Orebom, Alexander,Morsch, Thomas,Andersson, Pher G.

supporting information, p. 11930 - 11935 (2016/10/07)

A number of cyclic olefins were prepared and evaluated for the asymmetric hydrogenation reaction using novel N,P-ligated iridium imidazole-based catalysts (Crabtree type). The diversity of these cyclic olefins spanned those having little functionality to

Birch reaction followed by asymmetric iridium-catalysed hydrogenation

Cadu, Alban,Paptchikhine, Alexander,Andersson, Pher G.

experimental part, p. 3796 - 3800 (2012/01/06)

Birch reaction products are asymmetrically hydrogenated with high enantio- and diastereoselectivity via iridium catalysts. This new method of producing chiral compounds was explored for a variety of 1,3-di- and 1,2,4-tri-substituted cyclohexadienes. Georg

Sequential Birch reaction and asymmetric Ir-catalyzed hydrogenation as a route to chiral building blocks

Paptchikhine, Alexander,Itto, Kaori,Andersson, Pher G.

supporting information; experimental part, p. 3989 - 3991 (2011/06/09)

A range of 1,2,4-trisubstituted cyclohexadienes obtained from the Birch reaction were hydrogenated asymmetrically to produce synthetically valuable chiral compounds in high enantio- and diastereoselectivity. The Royal Society of Chemistry.

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