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Prop-2-en-1-yl 1-oxaspiro[2.5]octane-2-carboxylate is a complex organic chemical compound with the molecular formula C11H16O3. It is a derivative of the spiro compound class, which consists of two cyclic structures connected by a single atom. In this case, the compound features a spiro[2.5]octane ring system with a carboxylate group and a prop-2-en-1-yl side chain. This molecule is known for its unique structure and potential applications in various chemical and pharmaceutical industries. Due to its specific arrangement of atoms and functional groups, prop-2-en-1-yl 1-oxaspiro[2.5]octane-2-carboxylate may exhibit distinct chemical properties and reactivity compared to other related compounds.

2916-10-1

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2916-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2916-10-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2916-10:
(6*2)+(5*9)+(4*1)+(3*6)+(2*1)+(1*0)=81
81 % 10 = 1
So 2916-10-1 is a valid CAS Registry Number.

2916-10-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name prop-2-enyl 1-oxaspiro[2.5]octane-2-carboxylate

1.2 Other means of identification

Product number -
Other names prop-2-en-1-yl 1-oxaspiro[2.5]octane-2-carboxylate

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:2916-10-1 SDS

2916-10-1Downstream Products

2916-10-1Relevant academic research and scientific papers

P(RNCH2CH2)3N: Efficient catalysts for transesterifications, acylations, and deacylations

Ilankumaran, Palanichamy,Verkade

, p. 3086 - 3089 (2007/10/03)

Extremely strong nonionic superbases of the type P(RNCH2CH2)3N catalyze the transesterification of carboxylic acid esters with high selectivity and yields at 25 °C. These bases also catalyze the deacetylation of alcohols under mild conditions in quantitative yields. Using enol acetates as acylating agents, primary and secondary alcohols are efficiently protected as acetates through the action of these catalysts. Substituents such as epoxide, carbamate, acetal, oxazoline, nitro, and alkynyl functionalities are tolerated under the reaction conditions. N-Protected peptides undergo clean transesterification without significant racemization, making this methodology potentially very useful.

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