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(S)-(-)-1-(2-METHOXYBENZOYL)-2-PYRROLIDINEMETHANOL, commonly known as Ropivacaine, is a local anesthetic medication that is used to numb specific areas of the body during surgical or medical procedures. It is a member of the amino amide class of local anesthetics and is known for its lower risk of toxicity compared to other similar medications. Ropivacaine works by blocking the transmission of pain signals from the nerves to the brain, making it a popular choice for both minor and major surgical procedures.

102069-83-0

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  • Methanone,[(2S)-2-(hydroxymethyl)-1-pyrrolidinyl](2-methoxyphenyl)-

    Cas No: 102069-83-0

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102069-83-0 Usage

Uses

Used in Medical and Surgical Procedures:
(S)-(-)-1-(2-METHOXYBENZOYL)-2-PYRROLIDINEMETHANOL is used as a local anesthetic agent for [application reason] to numb specific areas of the body during surgical or medical procedures, providing pain relief and ensuring patient comfort.
Used in Epidural Anesthesia for Childbirth:
(S)-(-)-1-(2-METHOXYBENZOYL)-2-PYRROLIDINEMETHANOL is used as an epidural anesthetic agent for [application reason] to provide pain relief during childbirth, allowing mothers to have a more comfortable and controlled labor experience.
Used in Nerve Block for Pain Management:
(S)-(-)-1-(2-METHOXYBENZOYL)-2-PYRROLIDINEMETHANOL is used as a nerve block agent for [application reason] to manage pain in various medical conditions, such as postoperative pain, chronic pain, or pain associated with certain medical procedures.
Used in Local Anesthesia in Surgeries:
(S)-(-)-1-(2-METHOXYBENZOYL)-2-PYRROLIDINEMETHANOL is used as a local anesthetic agent for [application reason] to provide pain relief during surgical procedures, ensuring patient comfort and facilitating the surgical process.
Used in the Pharmaceutical Industry:
(S)-(-)-1-(2-METHOXYBENZOYL)-2-PYRROLIDINEMETHANOL is used as a key ingredient in the development of pharmaceutical products for [application reason] to treat various medical conditions that require pain management and local anesthesia.

Check Digit Verification of cas no

The CAS Registry Mumber 102069-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,0,6 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 102069-83:
(8*1)+(7*0)+(6*2)+(5*0)+(4*6)+(3*9)+(2*8)+(1*3)=90
90 % 10 = 0
So 102069-83-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H17NO3/c1-17-12-7-3-2-6-11(12)13(16)14-8-4-5-10(14)9-15/h2-3,6-7,10,15H,4-5,8-9H2,1H3/t10-/m0/s1

102069-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2S)-2-(hydroxymethyl)pyrrolidin-1-yl]-(2-methoxyphenyl)methanone

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:102069-83-0 SDS

102069-83-0Relevant articles and documents

THE ENANTIOSELECTIVE CONVERSION OF ORTHO-SUBSTITUTED BENZOIC ACIDS TO CHIRAL CYCLOHEXANE DERIVATIVES

Schultz, Arthur G.,Sundararaman, Padmanabhan,Macielag, Mark,Lavieri, Frank P.,Welch, Martha

, p. 4575 - 4578 (2007/10/02)

The diastereoselectivity of reductive methylation of 1a-1c to give 2a-2c and 11 to give 12 is 260:1 and >99:1, respectively.

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