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2-anilino-1-methylcyclohexan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100072-35-3

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100072-35-3 Usage

Chemical properties

Tertiary amine derivative and aliphatic alcohol

Physical properties

White to light brown solid, molecular weight of 235.36 g/mol

Uses

Pharmaceutical intermediate for the synthesis of various drugs (such as antihypertensive and antiarrhythmic medications), antioxidant in rubber and plastics

Applications

Pharmaceutical, agrochemical, and polymer industries

Check Digit Verification of cas no

The CAS Registry Mumber 100072-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,0,7 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100072-35:
(8*1)+(7*0)+(6*0)+(5*0)+(4*7)+(3*2)+(2*3)+(1*5)=53
53 % 10 = 3
So 100072-35-3 is a valid CAS Registry Number.

100072-35-3Downstream Products

100072-35-3Relevant academic research and scientific papers

One-Pot Synthesis of N-Substituted Alkylaminocyclohexanols by the Addition of Electrophiles Formed in situ in the System Н2О2 + HBr (HCl)

Sadygov,Alimardanov, Kh. M.,Ismailova, Sh. I.,Babaev

, p. 650 - 657 (2018/06/14)

Highly selective one-pot synthesis of N-substituted aminocyclohexanols has been performed by hydroxyhalogenation of the corresponding cyclohexenes with electrophilic reagents formed in situ in the system Н2О2 + HHlg (Hlg = Cl, Br), with subsequent substitution of halogen atoms with amines. Some products were tested as antimicrobial additives to motor oils and cooling lubricants and showed high antibacterial and antifungal activity.

ZEOLITE-CATALYZED RING-OPENING OF EPOXIDES WITH AMINES

Onaka, Makoto,Kawai, Motomitsu,Izumi, Yusuke

, p. 779 - 782 (2007/10/02)

The ring-opening of unsymmetrical epoxedes with amines has been investigated using zeolite as a catalyst.Moderately acidic and basic zeolite shows higher catalytic activity and regioselectivity compared to strongly acidic or basic zeolite.The cooperative

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