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72845-85-3

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72845-85-3 Usage

Chemical Class

Dioxolane derivative

Alias

Isopropylphenidate

Usage

Commonly used as a stimulant and psychoactive drug for recreational purposes

Classification

Substituted phenethylamine

Similarity

Shares properties with other psychoactive substances such as MDMA and amphetamines

Effects

Known for its stimulant and euphoric effects

Recreational Use

Often used for its psychoactive properties

Regulation

Use is regulated in many countries due to potential side effects and health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 72845-85-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,4 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72845-85:
(7*7)+(6*2)+(5*8)+(4*4)+(3*5)+(2*8)+(1*5)=153
153 % 10 = 3
So 72845-85-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H22O2/c1-11(2)14-6-4-13(5-7-14)10-12(3)15-16-8-9-17-15/h4-7,11-12,15H,8-10H2,1-3H3

72845-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[1-(4-propan-2-ylphenyl)propan-2-yl]-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names EINECS 276-935-5

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:72845-85-3 SDS

72845-85-3Downstream Products

72845-85-3Relevant articles and documents

Synthesis and perfume characteristics of acetals containing an aromatic ring

Vyglazov,Chuiko,Izotova,Vintarskaya,Yudenko

, p. 1888 - 1891 (2001)

Aromatic acetals were prepared by condensation of 2-methyl-3-(4-R-phenyl)propanals (R = Me, i-Pr, i-Bu) with ethanol, methanol, ethylene glycol, 1,2-propanediol, methyl Cellosolve, and Cellosolve. The perfume characteristics of the acetals were studied.

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