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3-Pentyn-1-amine, 5-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

918871-65-5

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918871-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 918871-65-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,8,7 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 918871-65:
(8*9)+(7*1)+(6*8)+(5*8)+(4*7)+(3*1)+(2*6)+(1*5)=215
215 % 10 = 5
So 918871-65-5 is a valid CAS Registry Number.

918871-65-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenylpent-3-yn-1-amine

1.2 Other means of identification

Product number -
Other names 3-Pentyn-1-amine,5-phenyl

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:918871-65-5 SDS

918871-65-5Upstream product

918871-65-5Downstream Products

918871-65-5Relevant academic research and scientific papers

Palladium(II)-Catalyzed Regioselective syn-Hydroarylation of Disubstituted Alkynes Using a Removable Directing Group

Liu, Zhen,Derosa, Joseph,Engle, Keary M.

, p. 13076 - 13081 (2016)

A palladium(II)-catalyzed regioselective syn-hydroarylation reaction of homopropargyl amines has been developed, wherein selectivity is controlled by a cleavable bidentate directing group. Under the optimized reaction conditions, both dialkyl and alkylaryl alkyne substrates were found to undergo hydroarylation with high selectivity. The products of this reaction contain a 4,4-disubstituted homoallylic amine motif that is commonly seen in drug molecules and other bioactive compounds.

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