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1603-61-8

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1603-61-8 Usage

Compound category

Aromatic hydrocarbons

Structural formation

Phenyl group attached to the second carbon atom of a cyclohexyl ring

Common uses

Production of organic compounds, precursor in synthesis of pharmaceuticals, agrochemicals, and specialty chemicals

Molecular stability

Stable molecular structure

Toxicity

Low toxicity in comparison to similar compounds

Industrial and research applications

Useful substance for industrial and research purposes

Potential applications

Development of new materials and technologies due to unique chemical properties

Check Digit Verification of cas no

The CAS Registry Mumber 1603-61-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1603-61:
(6*1)+(5*6)+(4*0)+(3*3)+(2*6)+(1*1)=58
58 % 10 = 8
So 1603-61-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H20/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1,3-4,7-8,14H,2,5-6,9-12H2

1603-61-8SDS

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-Cyclohexyl-2-phenylethane

1.2 Other means of identification

Product number -
Other names 1-Cyclohexyl-2-phenyl-aethan

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:1603-61-8 SDS

1603-61-8Relevant articles and documents

Synthesis of lactate derivatives via reductive radical addition to α-oxyacrylates

Diccianni, Justin B.,Chin, Mason,Diao, Tianning

, p. 4180 - 4185 (2019)

Lactate derivatives are important synthetic precursors to a variety of pharmaceutical products. Previously reported methods to prepare lactates require multiple steps or have limited scopes. Herein, we report a Ni-catalyzed reductive addition of a variety

Nickel-catalyzed cross-coupling of umpolung carbonyls and alkyl halides

Zhu, Dianhu,Lv, Leiyang,Qiu, Zihang,Li, Chao-Jun

, (2019/05/22)

An effective nickel-catalyzed cross-coupling of Umpolung carbonyls and alkyl halides was developed. Complementary to classical alkylation techniques, this reaction utilizes Umpolung carbonyls as the environmentally benign alkyl nucleophiles, providing an efficient and selective catalytic alternative to the traditional use of highly reactive alkyl organometallic reagents.

Synthesis of quinolinyl-based pincer copper(ii) complexes: an efficient catalyst system for Kumada coupling of alkyl chlorides and bromides with alkyl Grignard reagents

Pandiri, Hanumanprasad,Gonnade, Rajesh G.,Punji, Benudhar

supporting information, p. 16747 - 16754 (2018/12/05)

Quinolinamide-based pincer copper(ii) complexes, κN,κN,κN-{C9H6N-(μ-N)-C(O)CH2NEt2}CuX [(QNNNEt2)CuX (X = Cl, 2; X = Br, 3; X = OAc, 4)], were synthesized by the reaction of ligand (QNNNEt2)-H (1) with CuX2 (X = Cl, Br or OAc) in the presence of Et3N. The reaction of (QNNNEt2)-H with CuX (X = Cl, Br or OAc) also afforded the Cu(ii) complexes 2, 3 and 4, respectively, instead of the expected Cu(i) pincer complexes. The formation of Cu(ii) complexes from Cu(i) precursors most likely occurred via the disproportionation reaction of Cu(i) into Cu(0) and Cu(ii). A cationic complex [(QNNNEt2)Cu(CH3CN)]OTf (5) was synthesized by the treatment of neutral complex 2 with AgOTf. On the other hand, the reaction of (QNNNEt2)-H (1) with [Cu(MeCN)4]ClO4 produced cationic Cu(i) complex, [(QNN(H)NEt2)Cu(CH3CN)]ClO4 (6), in good yield. All complexes 2-5 were characterized by elemental analysis and HRMS measurements. Furthermore, the molecular structures of 2, 3 and 4 were elucidated by X-ray crystallography. Complex 4 crystallizes in a dimeric and catemeric pattern. The cationic complex 5 was found to be an efficient catalyst for the Kumada coupling reaction of diverse nonactivated alkyl chlorides and bromides with alkyl magnesium chloride under mild reaction conditions.

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