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24190-33-8

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24190-33-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24190-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,1,9 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24190-33:
(7*2)+(6*4)+(5*1)+(4*9)+(3*0)+(2*3)+(1*3)=88
88 % 10 = 8
So 24190-33-8 is a valid CAS Registry Number.

24190-33-8SDS

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 4-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]butan-2-one

1.2 Other means of identification

Product number -
Other names (+)-γ-dihydroionone

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:24190-33-8 SDS

24190-33-8Relevant articles and documents

Stoll,Hinder

, p. 1859,1860 Anm. 1 (1954)

Dotofide, a guanidine-interrupted terpenoid from the marine slug doto pinnatifida (Gastropoda, Nudibranchia)

Putz, Annika,Kehraus, Stefan,Diaz-Agras, Guillermo,Waegele, Heike,Koenig, Gabriele M.

, p. 3733 - 3737 (2011)

An unusual natural product (dotofide, 1), in which the terpenoid skeleton is interrupted by a guanidine moiety was obtained from the marine slug Doto pinnatifida. The absolute configuration of compound 1 was deduced by ozonolysis and subsequent CD spectro

Ruzicka et al.

, p. 1740,1751 (1948)

Bioactive compounds with added value prepared from terpenes contained in solid wastes from the olive oil industry

Parra, Andres,Lopez, Pilar E.,Garcia-Granados, Andres

experimental part, p. 421 - 439 (2010/09/05)

Starting from solid wastes from two-phase olive-oil extraction, the pentacyclic triterpenes oleanolic acid and maslinic acid were isolated. These natural compounds were transformed into methyl olean-12-en-28-oate (5), which then was transformed into several seco-C-ring triterpene compounds by chemical and photolytic modifications. The triene seco-products were fragmented through several oxidative procedures to produce, simultaneously, cis- and trans-decalin derivatives, both potential synthons for bioactive compounds. The chemical behavior of the isolated fragments was investigated, and a suitable approach to several low-molecular-weight terpenes was performed. These are interesting processes for the value-addition to solid waste from the olive-oil industry.

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