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25784-00-3

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25784-00-3 Usage

Functionality

Local anesthetic

Mechanism of Action

Blocks transmission of nerve signals

Applications

Medical and dental procedures, minor surgical procedures, spinal anesthesia

Form

Amino benzoic acid ester

Common combinations

With epinephrine to prolong effects

Administration

Injection

Duration of Action

Short

Safety and Efficacy

Considered safe and effective when used appropriately.

Check Digit Verification of cas no

The CAS Registry Mumber 25784-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,7,8 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25784-00:
(7*2)+(6*5)+(5*7)+(4*8)+(3*4)+(2*0)+(1*0)=123
123 % 10 = 3
So 25784-00-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO3/c11-6-5-10-8-4-2-1-3-7(8)9(12)13/h1-4,10-11H,5-6H2,(H,12,13)

25784-00-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-hydroxyethylamino)benzoic acid

1.2 Other means of identification

Product number -
Other names 2-(1,8-NAPHTHYRIDIN-2-YL)PHENOL

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:25784-00-3 SDS

25784-00-3Downstream Products

25784-00-3Relevant articles and documents

Synthesis of isocoumarins via Pd/C-mediated reactions of o-iodobenzoic acid with terminal alkynes

Subramanian, Venkataraman,Batchu, Venkateswara Rao,Barange, Deepak,Pal, Manojit

, p. 4778 - 4783 (2007/10/03)

The coupling reaction of o-iodobenzoic acid with terminal alkynes by using a catalyst system of 10% Pd/C-Et3N-CuI-PPh3 has been studied in a variety of solvents. 3-Substituted isocoumarins were formed in good yields and with good reg

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