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66504-75-4

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66504-75-4 Usage

Chemical Properties

Off-White Solid

Check Digit Verification of cas no

The CAS Registry Mumber 66504-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,0 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 66504-75:
(7*6)+(6*6)+(5*5)+(4*0)+(3*4)+(2*7)+(1*5)=134
134 % 10 = 4
So 66504-75-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H15N.ClH/c1-9-2-4-10(5-3-9)12-6-11(12)7-13-8-12;/h2-5,11,13H,6-8H2,1H3;1H

66504-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Bicifadine Hydrochloride

1.2 Other means of identification

Product number -
Other names BICIFADINE

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:66504-75-4 SDS

66504-75-4Relevant articles and documents

METHODS AND COMPOSITIONS FOR THE TREATMENT OF URINARY INCONTINENCE

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, (2008/06/13)

Methods and compositions containing bicifadine are provided for the prevention and treatment of lower urinary tract disorders in mammalian subjects. The methods and compositions may be used to prevent or treat urinary incontinence, urinary urgency, noctur

Polymorphs of bicifadine hydrochloride

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Page 5, (2008/06/13)

A new polymorphic crystalline form of bicifadine hydrochloride, designated form B, which is more thermodynamically stable than the previously known polymorphic form of bicifadine hydrochloride, designated as form A, methods for preparing said crystalline

Process for resolving cis-1-substituted phenyl-1,2-cyclopropanedicarboxylic acids

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, (2008/06/13)

A method for resolving racemic substituted cyclopropanedicarboxylic acids which are useful as intermediates for the preparation of substituted phenyl azabicyclohexanes which possess anxyolitic and analgesic activity.

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