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N-acetylprocaine is a chemical compound derived from procaine, an ester-type local anesthetic. It is formed by the acetylation of procaine, which involves the addition of an acetyl group to the molecule. This modification enhances the duration of action and reduces the rate of hydrolysis, making N-acetylprocaine a longer-acting anesthetic compared to its parent compound. It is used in medical procedures to numb specific areas of the body, providing pain relief during surgeries or other invasive treatments. The chemical structure of N-acetylprocaine allows it to block nerve impulses, effectively preventing the sensation of pain.

6062-23-3

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6062-23-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6062-23-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,6 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6062-23:
(6*6)+(5*0)+(4*6)+(3*2)+(2*2)+(1*3)=73
73 % 10 = 3
So 6062-23-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H22N2O3/c1-4-17(5-2)10-11-20-15(19)13-6-8-14(9-7-13)16-12(3)18/h6-9H,4-5,10-11H2,1-3H3,(H,16,18)

6062-23-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(diethylamino)ethyl 4-acetamidobenzoate

1.2 Other means of identification

Product number -
Other names 2-diethylaminoethyl 4-acetamidobenzoate

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:6062-23-3 SDS

6062-23-3Downstream Products

6062-23-3Relevant academic research and scientific papers

Specificity of esterases and structure of prodrug esters: Reactivity of various acylated acetaminophen compounds and acetylaminobenzoated compounds

Seki,Kawaguchi,Higuchi

, p. 855 - 860 (2007/10/02)

The relative rates of enzymatically catalyzed hydrolysis of various esters of p-acetylaminobenzoic acid (APAB) and variously acylated acetaminophen (APAP) derivatives were measured. Neutral, anionic, and cationic esters were examined. The enzyme sources adopted were rat intestinal homogenate, rat liver homogenate, rat plasma, and a partly purified commercial enzyme. In both APAB and APAP esters, neutral esters were the most sensitive of the enzyme sources examined, and the sensitivity was due to the carbon chain length. The APAP esters were enzymatically more stable than the APAP esters. The relative rates of hydrolysis of these esters varied depending on the enzyme source. The ability of structure recognition was good in rat intestinal homogenate, but weak in rat plasma. These results suggest that ester prodrugs can be designed to cleave preferentially at selected sites along the pathway between absorption and disposition in the body.

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