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16728-47-5

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16728-47-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16728-47-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,2 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16728-47:
(7*1)+(6*6)+(5*7)+(4*2)+(3*8)+(2*4)+(1*7)=125
125 % 10 = 5
So 16728-47-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO/c1-2-3-4-7-10-8-5-6-9/h2-5,7-8H2,1H3

16728-47-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-pentoxypropanenitrile

1.2 Other means of identification

Product number -
Other names 3-pentyloxy-propionitrile

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:16728-47-5 SDS

16728-47-5Downstream Products

16728-47-5Relevant articles and documents

Synthesis and fluorescence studies on menthol-coumarin conjugates

Rao, H. Surya Prakash,Desai, Avinash

, p. 514 - 524 (2015/07/07)

A three-step protocol for synthesis of alcohol containing aliphatic natural products and coumarins has been described. The Blaise reaction of converting the nitrile to β-keto esters formed key-step in this protocol. The menthol-coumarin conjugates prepared for the first time are subjected to absorption and fluorescence emission studies. The studies reveal that menthol substitution has little influence on the absorption or emission characteristic of the chromophore. However, substitution of C(6)H or C(6)OMe of the coumarin with NEt2 has dramatic influence on both absorption and emission of the conjugate. Solvatochromic studies and analysis of Stoke shift data show that the menthol-coumarin conjugate with C(6)NEt2 stabilizes itself in dipolar push-pull structure in ground and excited states.

Increased efficacies of an individual catalytic site in clustered multivalent dendritic catalysts

Jayamurugan, Govindasamy,Jayaraman, Narayanaswamy

supporting information; experimental part, p. 2379 - 2390 (2009/12/28)

In the studies reported so far on dendrimer-mediated catalysis, the efficacies of the catalytic units were studied and compared primarily across the generations. In order to identify the efficacy of an individual catalytic unit with respect to the number

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