Cas 1200678-99-4,5-(2-methylbut-3-en-2-yl)-1-(2-nitrobenzyl)-1H-imidazole-4-carbaldehyde

1200678-99-4

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Basic information

Product Name: 5-(2-methylbut-3-en-2-yl)-1-(2-nitrobenzyl)-1H-imidazole-4-carbaldehyde
Synonyms: 5-(2-methylbut-3-en-2-yl)-1-(2-nitrobenzyl)-1H-imidazole-4-carbaldehyde
CAS NO:1200678-99-4
Molecular Formula:
Molecular Weight: 299.329
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-(2-methylbut-3-en-2-yl)-1-(2-nitrobenzyl)-1H-imidazole-4-carbaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: 5-(2-methylbut-3-en-2-yl)-1-(2-nitrobenzyl)-1H-imidazole-4-carbaldehyde(1200678-99-4)
EPA Substance Registry System: 5-(2-methylbut-3-en-2-yl)-1-(2-nitrobenzyl)-1H-imidazole-4-carbaldehyde(1200678-99-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1200678-99-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1200678-99-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,0,6,7 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1200678-99:
(9*1)+(8*2)+(7*0)+(6*0)+(5*6)+(4*7)+(3*8)+(2*9)+(1*9)=134
134 % 10 = 4
So 1200678-99-4 is a valid CAS Registry Number.

1200678-99-4Upstream product

1200679-25-9 (5-(2-methylbut-3-en-2-yl)-1-(2-nitrobenzyl)-1H-imidazol-4-yl)methanol

1200678-99-4Downstream Products

1200679-04-4 C₂₄H₃₂N₄O₇

1200678-99-4Relevant academic research and scientific papers

Total synthesis of isoroquefortine E and phenylahistin

Shangguan, Ning,Joullié, Madeleine M.

supporting information; experimental part, p. 6755 - 6757 (2010/04/27)

Isoroquefortine E and phenylahistin were synthesized using the Horner-Wadsworth-Emmons reaction as the key step to build the dehydroamino acid moiety. The syntheses provided the materials for the biological studies of the roquefortine-phenylahistin molecu

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