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16409-44-2

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16409-44-2 Usage

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 16409-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,0 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16409-44:
(7*1)+(6*6)+(5*4)+(4*0)+(3*9)+(2*4)+(1*4)=102
102 % 10 = 2
So 16409-44-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O2/c1-10(2)6-5-7-11(3)8-9-14-12(4)13/h6,8H,5,7,9H2,1-4H3/b11-8+

16409-44-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name GERANYL ACETATE

1.2 Other means of identification

Product number -
Other names 2,6-Octadien-1-ol, 3,7-dimethyl-, acetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Odor agents
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:16409-44-2 SDS

16409-44-2Related news

Enzymatic synthesis of GERANYL ACETATE (cas 16409-44-2) in packed bed reactor in supercritical carbon dioxide under various pressure-temperature conditions and reactor configurations08/07/2019

As an alternative to the chemical synthesis of geranyl acetate, the aim of the present study is to better understand its enzymatic synthesis in a 1 mL packed bed reactor (PBR) using supercritical CO2 as a green solvent and immobilized lipase B from Candida antarctica as a catalyst. Using a full ...detailed

16409-44-2Relevant articles and documents

Rapid biomimetic total synthesis of (±)-rossinone B

Zhang, Ziyang,Chen, Jiahua,Yang, Zhen,Tang, Yefeng

, p. 5554 - 5557 (2010)

A biomimetic total synthesis of (±)-rossinone B has been achieved through a highly efficient strategy featuring a series of rationally designed reactions, including a one-pot allylic rearrangement/oxidation reaction to generate the vinyl quinone 27, an intramolecular vinyl quinone Diels-Alder reaction to construct the linear 6-6-5 tricyclic core of 28, and a double conjugate addition/β-elimination cascade to complete the total synthesis of 1.

Formamide catalyzed activation of carboxylic acids-versatile and cost-efficient amidation and esterification

Huy, Peter H.,Mbouhom, Christelle

, p. 7399 - 7406 (2019/08/20)

A novel, broadly applicable method for amide C-N and ester C-O bond formation is presented based on formylpyrrolidine (FPyr) as a Lewis base catalyst. Herein, trichlorotriazine (TCT), which is the most cost-efficient reagent for OH-group activation, was employed in amounts of ≤40 mol% with respect to the starting material (100 mol%). The new approach is distinguished by excellent cost-efficiency, waste-balance (E-factor down to 3) and scalability (up to >80 g). Moreover, high levels of functional group compatibility, which includes acid-labile acetals and silyl ethers, are demonstrated and even peptide C-N bonds can be formed. In comparison to reported amidation procedures using TCT, yields are considerably improved (for instance from 26 to 91%) and esterification is facilitated for the first time in synthetically useful yields. These significant enhancements are rationalized by activation by means of acid chlorides instead of less electrophilic acid anhydride intermediates.

Highly Active Manganese-Mediated Acylation of Alcohols with Acid Chlorides or Anhydrides

Joo, Seong-Ryu,Youn, Young-Jin,Hwang, Young-Ran,Kim, Seung-Hoi

, p. 2665 - 2669 (2017/10/07)

To explore further the practical uses of highly active manganese (Mn?), a variety of alcohols were treated with Mn?, and the resulting complexes were coupled with acid chlorides and/or acetic anhydride in the absence of any extra catalyst. The subsequent reactions took place smoothly under mild conditions, providing the corresponding O-acylation products in good to excellent isolated yields.

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