Welcome to LookChem.com Sign In|Join Free

CAS

  • or

117332-89-5

Post Buying Request

117332-89-5 Suppliers

Recommended suppliersmore

This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

117332-89-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117332-89-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,3,3 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 117332-89:
(8*1)+(7*1)+(6*7)+(5*3)+(4*3)+(3*2)+(2*8)+(1*9)=115
115 % 10 = 5
So 117332-89-5 is a valid CAS Registry Number.

117332-89-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Acetyl fentanyl hydrochloride

1.2 Other means of identification

Product number -
Other names N-(1-phenethylpiperidin-4-yl)-N-phenylacetamide hydrochloride

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:117332-89-5 SDS

117332-89-5Relevant articles and documents

An efficient, optimized synthesis of fentanyl and related analogs

Valdez, Carlos A.,Leif, Roald N.,Mayer, Brian P.

, (2015/02/19)

The alternate and optimized syntheses of the parent opioid fentanyl and its analogs are described. The routes presented exhibit high-yielding transformations leading to these powerful analgesics after optimization studies were carried out for each synthetic step. The general three-step strategy produced a panel of four fentanyls in excellent yields (73-78%) along with their more commonly encountered hydrochloride and citric acid salts. The following strategy offers the opportunity for the gram-scale, efficient production of this interesting class of opioid alkaloids.