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2(1H)-Isoquinolinehexanol, 3,4-dihydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88014-18-0

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88014-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88014-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,1 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88014-18:
(7*8)+(6*8)+(5*0)+(4*1)+(3*4)+(2*1)+(1*8)=130
130 % 10 = 0
So 88014-18-0 is a valid CAS Registry Number.

88014-18-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(3,4-dihydro-1H-isoquinolin-2-yl)hexan-1-ol

1.2 Other means of identification

Product number -
Other names -

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:88014-18-0 SDS

88014-18-0Downstream Products

88014-18-0Relevant academic research and scientific papers

THE SYNTHESIS OF SOME ALCOHOLS DERIVED FROM 1,2,3,4-TETRAHYDROISOQUINOLINE AND FROM 1,2,3,4-TETRAHYDROQUINOLINE

Ferles, Miloslav,Silhankova, Alexandra,Kafka, Stanislav,Taufmann, Petr,Motacek, Tomas

, p. 1759 - 1764 (2007/10/02)

Reduction of ethyl ester of ω-(1,2,3,4-tetrahydro-2-isoquinolyl)alkanoic acids IVa-e by means of LiAlH4 was used for the preparation of corresponding primary alcohols Ia-e. 6-(1,2,3,4-tetrahydro-2-isoquinolyl)-1-hexanol (Ie) was also obtained on reduction of ester amide VII.Reduction of 2-(2-hydroxypropanoyl)-1,2,3,4-tetrahydroisoquinoline (V) with LiAlH4 gave secondary alcohol II; in the quinoline series alcohol IIIa was obtained in a similar manner by reduction of ethyl 3-(1,2,3,4-tetrahydro-1-quinolyl)propanoate (IIIb).

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