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1620-30-0

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1620-30-0 Usage

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 27, p. 1903, 1990 DOI: 10.1002/jhet.5570270711

Check Digit Verification of cas no

The CAS Registry Mumber 1620-30-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1620-30:
(6*1)+(5*6)+(4*2)+(3*0)+(2*3)+(1*0)=50
50 % 10 = 0
So 1620-30-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H15NO/c20-18(15-7-3-1-4-8-15,16-9-5-2-6-10-16)17-11-13-19-14-12-17/h1-14,20H

1620-30-0 Well-known Company Product Price

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  • Aldrich

  • (121983)  α-(4-Pyridyl)benzhydrol  75%, technical grade

  • 1620-30-0

  • 121983-25G

  • 1,577.16CNY

  • Detail

1620-30-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name diphenyl(pyridin-4-yl)methanol

1.2 Other means of identification

Product number -
Other names diphenyl-4-pyridylmethan-1-ol

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:1620-30-0 SDS

1620-30-0Relevant articles and documents

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Mislow

, p. 2559 (1947)

-

-

Vittimberga et al.

, p. 4397 (1975)

-

Preparation method of alpha, alpha-diphenyl-4-piperidine methanol

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Paragraph 0028-0030; 0037-0039; 0046-0048; 0055-0057, (2021/05/01)

The invention discloses a preparation method of alpha, alpha-diphenyl-4-piperidine methanol, which comprises the following steps of by using benzophenone and 4-cyanopyridine as raw materials, carrying out free radical coupling reaction under the action of alkali metal to obtain alpha, alpha-diphenyl-4-piperidine methanol, reacting the obtained alpha, alpha-diphenyl-4-pyridine methanol with a benzylation reagent to generate N-benzyl-alpha, alpha-diphenyl-4-pyridine methanol, carrying out hydroboration reduction on the N-benzyl-alpha, alpha-diphenyl-4-pyridine methanol to obtain (1-benzyl-1, 2, 3, 6-tetrahydropyridine-4-yl)benzhydrol, ane enabling (1-benzyl-1, 2, 3, 6-tetrahydropyridine-4-yl)benzhydrol to be subjected to catalytic hydrogenation and debenzylation protection to obtain alpha, alpha-diphenyl-4-piperidine methanol. The method has the advantages of cheap and accessible raw materials, high reaction yield and high controllability, and is suitable for industrial production requirements.

Preparation method of diphenyl(4-pyridyl)methanol

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Paragraph 0010, (2019/10/02)

The invention relates to a preparation method of diphenyl(4-pyridyl)methanol. According to the method, benzophenone and 4-cyanopyridine are taken as raw materials to carrying out a one-step reaction to prepare the diphenyl(4-pyridyl)methanol. The preparation method is simple in process, low in cost, high in yield and high in controllability, and is suitable for industrial production.

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