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440083-00-1

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440083-00-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 440083-00-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,0,0,8 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 440083-00:
(8*4)+(7*4)+(6*0)+(5*0)+(4*8)+(3*3)+(2*0)+(1*0)=101
101 % 10 = 1
So 440083-00-1 is a valid CAS Registry Number.

440083-00-1SDS

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 (2R,3S,6R,7S)-2,7-Diallyl-oxepane-3,6-diol

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:440083-00-1 SDS

440083-00-1Downstream Products

440083-00-1Relevant articles and documents

Synthesis and biological studies of flexible brevetoxin/ciguatoxin models with marked conformational preference

Candenas,Pinto, Francisco M,Cintado, Cristina G,Morales, Ezequiel Q,Brouard, Ignacio,Díaz, M.Teresa,Rico, Milagros,Rodríguez, Elsa,Rodríguez, Rosa M,Pérez, Ricardo,Pérez, Ruby L,Martín, Julio D

, p. 1921 - 1942 (2007/10/03)

A comparison of the more active polyether toxins which are selective activators of voltage-sensitive sodium channels (VSSC), indicate that these molecules are mostly flat, with a hinge part around the middle of the molecules and a large curvature at one of the ends. Assuming that the receptor is topographically complementary to the active molecules, from the result reported here we could conclude, that the specific requirements of the receptor region can be achieved by synthetic polyether models based on exclusive participation of oxane/oxepane moieties. A new convergent approach to give oxepene rings via double reduction of methyl diacetals is explored. In searching for biological models to further characterize Na+ channels, our studies show that different voltage-dependent Na+ channels are expressed in the rat uterus and activated by brevetoxin-B. However, selected compound models synthesized in this work, failed to inhibit or activate Na+ channel function.

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