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63058-26-4

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63058-26-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63058-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,5 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63058-26:
(7*6)+(6*3)+(5*0)+(4*5)+(3*8)+(2*2)+(1*6)=114
114 % 10 = 4
So 63058-26-4 is a valid CAS Registry Number.

63058-26-4SDS

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 Farnesylbromacetat

1.2 Other means of identification

Product number -
Other names Bromo-acetic acid (2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl ester

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:63058-26-4 SDS

63058-26-4Relevant articles and documents

Bio-inspired surfactants capable of generating plant volatiles

Bhadani, Avinash,Rane, Jayant,Veresmortean, Cristina,Banerjee, Sanjoy,John, George

, p. 3076 - 3082 (2015)

Plants are able to synthesize, store and release lipophilic organic molecules known as plant volatiles (PVs) utilizing specific biological pathways and different enzymes which play vital roles in the plant's defence and in dealing with biotic and abiotic stress situations. The process of generation, storage and release of PVs by plants acquired during the course of evolution is a very complex phenomenon. Bio-inspired molecular design of farnesol-based surfactants facilitates similar production, storage and release of PVs. The designed molecules adsorb at air-water interface and self-aggregate into micelles in aqueous system. The structural design of the molecules allows them to self-activate in water via intramolecular cation-π interactions. The activated molecules undergo molecular rearrangements generating volatile organic molecules both at interface and inside the micelle core. The molecules adsorbed at the interface initially release the formed volatile molecules creating vacant space at interface, thus thermodynamically directing the micelle to release the manufactured volatile products. This journal is

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