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6007-24-5

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6007-24-5 Usage

Physical state

Colorless, flammable liquid

Common use

Protecting group for aldehydes and ketones in organic synthesis

Property

Forms stable complexes with carbonyl compounds

Applications

a. Synthesis of pharmaceuticals
b. Synthesis of agrochemicals
c. Production of fragrances and flavoring compounds

Fields of potential application

a. Medicine
b. Agriculture
c. Perfumery

Reactivity

Versatile

Chemical properties

Unique

Check Digit Verification of cas no

The CAS Registry Mumber 6007-24-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,0 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6007-24:
(6*6)+(5*0)+(4*0)+(3*7)+(2*2)+(1*4)=65
65 % 10 = 5
So 6007-24-5 is a valid CAS Registry Number.

6007-24-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethyl-2-methyl-1,3-dithiane

1.2 Other means of identification

Product number -
Other names 1,3-Dithiane,2-ethyl-2-methyl

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:6007-24-5 SDS

6007-24-5Relevant articles and documents

Odorless thioacetalization reagent 2-[1,3] dithian-2-ylidene-3-oxo- butanamide and its chemoselectivity

Liu, Jun,Liu, Qun,Yu, Haifeng,Ouyang, Yan,Dong, Dewen

, p. 4545 - 4556 (2007/10/03)

2-[1,3]Dithian/dithiolan-2-ylidene-3-oxo-butanamide 2a/2b were synthesized and investigated in the thioacetalization reaction of aldehydes/ketones 3. The experiments revealed that 2a could be used as a nonthiolic, odorless 1,3-propanedithiol equivalent in the conversion of aldehydes/ketones into the corresponding dithianes 4, however, 2b was less effective. Moreover, the chemoselectivity of the thioacetalization of 3 in the presence of 2a is discussed.

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