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75033-21-5

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75033-21-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75033-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,3 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75033-21:
(7*7)+(6*5)+(5*0)+(4*3)+(3*3)+(2*2)+(1*1)=105
105 % 10 = 5
So 75033-21-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O3/c1-5-14-11(13)10-12(4,15-10)8-6-7-9(2)3/h7,10H,5-6,8H2,1-4H3

75033-21-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-methyl-3-(4-methylpent-3-enyl)oxirane-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2,3-Epoxy-3,7-dimethyl-oct-6-ensaeure-aethylester

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:75033-21-5 SDS

75033-21-5Relevant articles and documents

Preparation method of muskmelon aldehyde, muskmelon aldehyde and application thereof

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Paragraph 0077-0080, (2020/07/12)

The invention relates to a preparation method of muskmelon aldehyde, muskmelon aldehyde and an application thereof, the preparation method comprises the following steps: carrying out a Darzen condensation reaction on 6-methyl-5-heptene-2-ketone, chloroacetate and an acid-binding agent under the condition of adding a solvent and a phase transfer catalyst to obtain epoxy caprylate; and saponifying the obtained epoxy caprylate in an aqueous solution of alkali to generate corresponding salt, acidifying with acid to obtain 3, 7-dimethyl-6-ene-2, 3-epoxy caprylic acid, carrying out a reduced pressure decarboxylation reaction on 3, 7-dimethyl-6-ene-2, 3-epoxy caprylic acid, and adding a mixture composed of an antioxidant and a polymerization inhibitor to obtain the muskmelon aldehyde product. Theconditions of the preparation method are easier to control, the production is safer, the yield is higher, and the product purity is high.

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