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66399-06-2

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66399-06-2 Usage

Classification

Intravenous anesthetic agent

Properties

Hypnotic and Sedative: Induces rapid onset of anesthesia when administered intravenously.
Rapid Onset and Offset of Action: Ideal for quick induction and recovery from anesthesia.
Antiemetic and Antipruritic Effects: Useful in preventing and treating postoperative nausea, vomiting, and itching.

Side Effects

Hypotension: Lowers blood pressure.
Respiratory Depression: Reduces breathing rate and depth.
Potential for Abuse: Can be misused for recreational purposes.

Caution

Healthcare professionals should monitor and dose propofol carefully to minimize adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 66399-06-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,3,9 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66399-06:
(7*6)+(6*6)+(5*3)+(4*9)+(3*9)+(2*0)+(1*6)=162
162 % 10 = 2
So 66399-06-2 is a valid CAS Registry Number.

66399-06-2SDS

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 2-[(dipropylamino)methyl]isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names N-Dipropylaminomethyl-phthalimid

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:66399-06-2 SDS

66399-06-2Downstream Products

66399-06-2Relevant articles and documents

Photochemical Cyclisation of Phthalimide Mannich Bases

Coyle, John D.,Newport, Graham L.

, p. 93 - 96 (2007/10/02)

Ultraviolet irradiation of Mannich bases derived from phthalimide, formaldehyde, and a secondary amine leads to cyclised products containing a new imidazolidine ring.The reaction is much less efficient when the secondary amine has an aromatic group adjacent to the nitrogen atom.Exceptionally, the Mannich base derived from 3-pyrroline does not cyclise but undergoes an internal oxidation-reduction reaction to give a substituted pyrrole.

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