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36748-60-4

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36748-60-4 Usage

Appearance

Colorless liquid

Usage

a. Production of perfumes and fragrance products
b. Synthesis of various organic compounds
c. Manufacturing of industrial and consumer products (soaps, detergents, cosmetics)
d. Potential applications in the pharmaceutical industry
e. Intermediate in organic synthesis

Classification

Fragrance ingredient

Scent

Warm, woody, and floral

Check Digit Verification of cas no

The CAS Registry Mumber 36748-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,4 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36748-60:
(7*3)+(6*6)+(5*7)+(4*4)+(3*8)+(2*6)+(1*0)=144
144 % 10 = 4
So 36748-60-4 is a valid CAS Registry Number.

36748-60-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-isopropyl-1,2,3,4-tetrahydro-isoquinoline

1.2 Other means of identification

Product number -
Other names 1H-Pyrido[3,4-b]indole,2,3,4,9-tetrahydro-1-isopropyl

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:36748-60-4 SDS

36748-60-4Downstream Products

36748-60-4Relevant articles and documents

Anisochrony of Isopropyl Methyl Groups in 1-Isopropyl-Substituted Tetralins and Indans

Pourahmady, N.,Palaniswamy, V. A.,Eisenbraun, E. J.

, p. 670 - 671 (1983)

1-Isopropyl-5-methylindan, 1-isopropyl-7-methylindan and 1-isopropyl-1,2,3,4-tetrahydronaphthalene show a large anisochrony (magnetic non-equivalence) of the isopropyl methyl signals at room temperature in their 1H NMR spectra.A decrease in magnitude of this anisochrony is observed, in each case, in the temperature range 30-150 deg C.However, for 1-isopropyl-8-methyltetralin, the magnitude of the non-equivalence of the isopropyl methyl signals is unexpectedly small.These latter signals converge at 85 deg C and then diverge in the opposite direction over the range 85-150 deg C.This alteration in anisochrony with temperature change for all cases is observed as a continuous downfield migration of one signal which, in turn, results from variations in conformation populations.

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