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1236262-83-1

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1236262-83-1 Usage

Physical properties

white to off-white crystalline powder

Use

local anesthetic and analgesic agent

Mechanism of action

inhibits nerve conduction by blocking sodium channels in neuron membranes

Effects

reversible loss of sensation in the area where it is applied

Common applications

topical creams and ointments for relief of pain and discomfort associated with minor skin irritations, burns, and insect bites

Investigated use

reducing pain associated with medical procedures and surgeries

Check Digit Verification of cas no

The CAS Registry Mumber 1236262-83-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,6,2,6 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1236262-83:
(9*1)+(8*2)+(7*3)+(6*6)+(5*2)+(4*6)+(3*2)+(2*8)+(1*3)=141
141 % 10 = 1
So 1236262-83-1 is a valid CAS Registry Number.

1236262-83-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-N-benzyl-N,3-dimethylbutanamide hydrochloride

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:1236262-83-1 SDS

1236262-83-1Downstream Products

1236262-83-1Relevant articles and documents

Chiral Thioureas Promote Enantioselective Pictet-Spengler Cyclization by Stabilizing Every Intermediate and Transition State in the Carboxylic Acid-Catalyzed Reaction

Klausen, Rebekka S.,Kennedy, C. Rose,Hyde, Alan M.,Jacobsen, Eric N.

, p. 12299 - 12309 (2017/09/12)

An investigation of the mechanism of benzoic acid/thiourea co-catalysis in the asymmetric Pictet-Spengler reaction is reported. Kinetic, computational, and structure-activity relationship studies provide evidence that rearomatization via deprotonation of

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