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63834-79-7

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63834-79-7 Usage

General Description

1-Phenyl-2,2-diethyl-1,3-propanediol, also known as ethylphenidate, is a chemical compound with the molecular formula C14H21NO2. It is a stimulant that is structurally similar to amphetamines and is often used as a recreational drug. Ethylphenidate is known to increase levels of dopamine and norepinephrine in the brain, leading to feelings of increased energy, focus, and euphoria. It is also thought to have potential as a treatment for attention-deficit hyperactivity disorder (ADHD) and narcolepsy, although more research is needed to confirm its efficacy and safety for these uses. Ethylphenidate can be consumed orally, nasally, or through injection, and its effects can last for several hours. However, its use is associated with a range of potential side effects, including increased heart rate, hypertension, and anxiety. Additionally, there is a risk of addiction and abuse with long-term use of ethylphenidate.

Check Digit Verification of cas no

The CAS Registry Mumber 63834-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,3 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63834-79:
(7*6)+(6*3)+(5*8)+(4*3)+(3*4)+(2*7)+(1*9)=147
147 % 10 = 7
So 63834-79-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H20O2/c1-3-13(4-2,10-14)12(15)11-8-6-5-7-9-11/h5-9,12,14-15H,3-4,10H2,1-2H3

63834-79-7SDS

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 2,2-diethyl-1-phenylpropane-1,3-diol

1.2 Other means of identification

Product number -
Other names MC 2340

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:63834-79-7 SDS

63834-79-7Downstream Products

63834-79-7Relevant articles and documents

Asymmetric synthesis of highly substituted β-lactones by nucleophile-catalyzed [2+2] cycloadditions of disubstituted ketenes with aldehydes

Wilson, Jonathan E.,Fu, Gregory C.

, p. 6358 - 6360 (2007/10/03)

α,α-Disubstituted β-lactones can be obtained by the cycloaddition of the corresponding ketenes with aldehydes (see scheme). For the first time, a chiral PPY derivative, 1, serves as an efficient catalyst for the asymmetric synthesis of β-lactones (PPY = 4-pyrrolidin-1-ylpyridine). To date, this is the only catalyst that is effective for enantioselective cycloadditions of disubstituted ketenes with aldehydes. (Chemical equation presented).

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