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16647-10-2

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16647-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16647-10-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,4 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16647-10:
(7*1)+(6*6)+(5*6)+(4*4)+(3*7)+(2*1)+(1*0)=112
112 % 10 = 2
So 16647-10-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H32O/c1-15(2)9-6-10-16(3)11-7-12-17(4)13-8-14-18(5)19/h8,15-16H,6-7,9-12,14H2,1-5H3

16647-10-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,10,14-trimethylpentadeca-4,5-dien-2-one

1.2 Other means of identification

Product number -
Other names 6,10,14-trimethyl-4,5-pentadecadien-2-one

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:16647-10-2 SDS

16647-10-2Relevant articles and documents

Method for preparing unsaturated ketone

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Paragraph 0035-0038; 0047; 0048; 0051; 0052, (2019/04/04)

The invention discloses a method for preparing unsaturated ketone. According to the method, an unsaturated alcohol and 2-alkoxy propylene are adopted as raw materials, an acid resin in a fixed bed aremodified, a Saucy-Marbet reaction is carried out, and unsaturated ketone is synthesized with high selectivity and high yields. According to the method, the modified acid resin is adopted as a catalyst, the problem that a common acid resin is poor in catalysis effect is solved; in addition, a fixed bed reactor is adopted to catalyze reactions, separation of the catalyst from reaction products before and after reactions can be achieved, equipment corrosion and adverse influence of a great amount of acids upon later industrial aftertreatment can be avoided, and the method is an economic and efficient synthesis method.

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