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tert-butyl 4-oxaspiro[2.5]octane-5-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73806-22-1

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73806-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73806-22-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,0 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73806-22:
(7*7)+(6*3)+(5*8)+(4*0)+(3*6)+(2*2)+(1*2)=131
131 % 10 = 1
So 73806-22-1 is a valid CAS Registry Number.

73806-22-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Oxaspiro(2,5)octane-2-carboxylic acid, tert-butyl ester

1.2 Other means of identification

Product number -
Other names -

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:73806-22-1 SDS

73806-22-1Downstream Products

73806-22-1Relevant academic research and scientific papers

Solid sodium hydroxide - THF, convenient system for synthesis esters of glycidic acids by darzens condensation

Gadaj,Kowalkowska,Jonczyk

, p. 577 - 584 (2008/09/19)

Isopropyl- and tert-butylchloroacetate react with carbonyl compounds in the presence of powdered sodium hydroxide in THF, without a catalyst, giving substituted glycidates. The process is applied for preparation of glycidates from ketones, hitherto unavailable by phase-transfer catalyzed Darzens condensation.

A convenient synthesis of aziridine-2-carboxylic esters

Legters, Johan,Thijs, Lambertus,Zwanenburg, Binne

, p. 1 - 15 (2007/10/02)

Optically active oxirane-2-carboxylic esters, prepared from allylic alcohols employing the Sharpless epoxidation, were treated with sodium azide.The azido alcohols obtained were subsequently converted into aziridine-2-carboxylic esters by reaction with triphenylphosphine, in good yields and with high optical purity.Various racemic oxirane-2-carboxylic esters were subjected to the same sequence of reactions.

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