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3062-66-6

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3062-66-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3062-66-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,6 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3062-66:
(6*3)+(5*0)+(4*6)+(3*2)+(2*6)+(1*6)=66
66 % 10 = 6
So 3062-66-6 is a valid CAS Registry Number.

3062-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-octadecyl-furan

1.2 Other means of identification

Product number -
Other names 3-Octadecylmercapto-propionsaeure

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:3062-66-6 SDS

3062-66-6Downstream Products

3062-66-6Relevant articles and documents

Chiral Sulphur-containing Molecules in Langmuir-Blodgett Films

Georges, Christian,Lewis, T. John,Llewellyn, J. Patrick,Salvagno, Susanna,Taylor, D. Martin,et al.

, p. 1531 - 1542 (2007/10/02)

Long, straight alkane chains have been functionalised with sulphur-containing groups at the chain-end, near the chain-end and at the midchain.The behaviour of such compounds in Langmuir films has been investigated.Several gave stable monolayers from which molecular areas have been determined.Surface potential (ΔV) measurements carried out simultaneously with the pressure-area (?-A) isotherms provided an important insight into the surface behaviour of some of the compounds.On compression, changes in the ΔV-A characteristics were clearly visible, well before any significant changes occured in the ?-A curves.New evidence presented here suggests also that the previous interpretation of the ?-A behaviour of C10H21SO(CH2)10CO2H in terms of molecular orientation was incorrect, dissolution of the monolayer in the water subphase at higher pressure being the most likely explanation.Attempts at depositing chiral L.B. multilayers of (+)-C18H37SO-p-tolyl were not successful because of crystallite formation on te quartz support.Multilayers of (+)-S-octadecylcysteine were deposited successfully, albeit with a monolayer of stearic acid interposed every seven monolayers of the chiral compound.No optical rotation was observed in the films.

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