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19792-68-8

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19792-68-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19792-68-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,9 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19792-68:
(7*1)+(6*9)+(5*7)+(4*9)+(3*2)+(2*6)+(1*8)=158
158 % 10 = 8
So 19792-68-8 is a valid CAS Registry Number.
InChI:InChI=1/C35H40N4O6/c1-9-22-21(6)34(42)39-29(22)16-27-20(5)25(12-14-33(41)45-8)31(37-27)17-30-24(11-13-32(40)44-7)19(4)26(36-30)15-28-18(3)23(10-2)35(43)38-28/h9-10,15-16,36-37H,1-2,11-14,17H2,3-8H3,(H,38,43)(H,39,42)/b28-15-,29-16-

19792-68-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Bilirubin dimethyl ester

1.2 Other means of identification

Product number -
Other names (Z,Z)-bilirubindimethylester

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:19792-68-8 SDS

19792-68-8Related news

Conformational analysis of an optically active BILIRUBIN DIMETHYL ESTER (cas 19792-68-8) and bis-N,N-dimethyl amide by circular dichroism, NMR and molecular dynamics09/24/2019

The dimethyl ester and bis-N,N-dimethylamide of an optically active analog of bilirubin (ßS,ß′S-dimethylmesobilirubin-XIIIα) is stabilized in a ridge-tile conformation by intramolecular hydrogen bonding, as detected by 1H-NMR and CD spectroscopy. The ridge-tile shape is most evident in nonpola...detailed

19792-68-8Relevant articles and documents

Reduction of a Bilindione-10-Thiol-Adduct as a Model of the Reduction Step of the Biliverdin Reductase System

Falk, Heinz,Marko, Helmut

, p. 319 - 321 (1991)

Biliverdin dimethyl ester and its 10-thioethanol addition product are reduced by LiBH4 with similar reaction velocities as derived from NMR experiments.This reaction serves as a model of the biliverdin reductase system.According to this model the addition of the enzyme thiol group to position 10 of biliverdin primarily serves as the binding and orienting mode.It is obviously not intended as such to accelerate the velocity of the reduction step.

POLYMER BOUND PYRROLE COMPOUNDS- II. SYNTHESIS AND PROPERTIES OF POLYSTYRENE-BOUND LINEAR TETRAPYRROLE PIGMENTS AND RELATED 5(1H)-PYRROMETHENONES

Castan, Pilar,Giralt, Ernest,Perez, Juan C.,Ribo, Josef M.,Siscart, Nuria,Trull, Francesc R.

, p. 2593 - 2608 (2007/10/02)

The title chromophores have been reversibly and covalently attached to differently functionalized polystyrenes including the α-poly(styrene-co-divinylbenzene), and its desnitro derivate.The influence on the reaction

POLYMER BOUND PYRROLE COMPOUNDS. REVERSIBLE ANCHORING OF BILIRUBIN AND BILIVERDIN TO A POLYSTIRENE MATRIX

Giralt, Ernest,Ribo, Josep Ma.,Trull, Francesc R.

, p. 4145 - 4146 (2007/10/02)

Both bilirubin and biliverdin, via their cesium salts, have been covalently attached to an insoluble polystyrene matrix (the so-called Nbb-resin), some chemical transformations have been carried out upon the supported pigments, and the resulting products have been detached by alkaline methanol.

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