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5986-99-2

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5986-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5986-99-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,8 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5986-99:
(6*5)+(5*9)+(4*8)+(3*6)+(2*9)+(1*9)=152
152 % 10 = 2
So 5986-99-2 is a valid CAS Registry Number.

5986-99-2SDS

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 16β-piperidino-5-androstene-3β,17β-diol diacetate

1.2 Other means of identification

Product number -
Other names Acetic acid (3S,8R,9S,10R,13S,14S,16S,17R)-3-acetoxy-10,13-dimethyl-16-piperidin-1-yl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl ester

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:5986-99-2 SDS

5986-99-2Downstream Products

5986-99-2Relevant articles and documents

Synthesis and neuromuscular blocking activity of 16β-piperidinosteroidal derivatives

Jindal, Dharam Paul,Piplani, Poonam,Fajrak, Hassan,Prior, Chris,Marshall, Ian G

, p. 195 - 202 (2007/10/03)

The synthesis and pharmacological profiles of some new steroidal mono- and bisquaternary ammonium derivatives have been described. The compounds featured have been conceptually derived structurally from two lead structures: pancuronium bromide 1 and chandonium iodide 2. In vitro and in vivo neuromuscular blocking studies have indicated the monoquaternary compound 15 to be less active than the bisquaternary compounds 10 and 11. The compound 11 has been found to be more active than d-tubocurarine.

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