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821799-10-4

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821799-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 821799-10-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,1,7,9 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 821799-10:
(8*8)+(7*2)+(6*1)+(5*7)+(4*9)+(3*9)+(2*1)+(1*0)=184
184 % 10 = 4
So 821799-10-4 is a valid CAS Registry Number.

821799-10-4SDS

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 (1S,9S)-10,10-dimethyl-6-aza-tricyclo[7.1.1.02,7]undeca-2(7),3,5-trien-5-carbaldehyde

1.2 Other means of identification

Product number -
Other names (1S,9S)-10,10-Dimethyl-6-aza-tricyclo[7.1.1.02,7]undeca-2(7),3,5-triene-5-carbaldehyde

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:821799-10-4 SDS

821799-10-4Relevant academic research and scientific papers

Synthesis of a C2-symmetric chiral bipyridyldiol ligand and its application in the enantioselective addition of diethylzinc to substituted benzaldehydes

Chen, Yi-Jing,Lin, Rong-Xin,Chen, Chinpiao

, p. 3561 - 3571 (2007/10/03)

Herein the synthesis of a novel C2-symmetric ligand comprising of a central bipyridine-pinene-derived core and two functionalized diphenylmethanol subunits is described. [8′-(Hydroxy-diphenyl-methyl)-10, 10,10′,10′-tetramethyl-[5,5′]bi[6-aza-tr

Synthesis and characterization of highly conjugated, chiral bridging ligands

Sauers, Angela L.,Ho, Douglas M.,Bernhard, Stefan

, p. 8910 - 8915 (2007/10/03)

This paper describes the synthesis of four chiral derivatives of the electronically highly conjugated tetra-2-pyridylpyrazine (TPPZ) bridging ligand, which are denoted (R)- and (S)-4,5- and 5,6-pineno-tetra-2-pyridylpyrazine (PTPPZ). Preparation of these ligands was undertaken through the use of commercially available, enantiomerically pure (1R)- and (1S)-α-pinene, which was functionalized and subsequently employed in a Kroehnke pyridine synthesis involving a furan-substituted pyridinium salt to yield a chiral, furan-substituted pyridyl intermediate. Oxidative degradation and subsequent reduction of this furan led to a chiral, substituted 2-pyridylaldehyde, which underwent a pyridoin condensation followed by cyclization to produce the final PTPPZ ligands.

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