Cas 292819-44-4,2-(4-Carboxy-benzyl)-2-{(Z)-4-[(6-hydroxy-hexyl)-(2-nitro-benzenesulfonyl)-amino]-but-2-enyl}-malonic acid dimethyl ester

292819-44-4

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Basic information

Product Name: 2-(4-Carboxy-benzyl)-2-{(Z)-4-[(6-hydroxy-hexyl)-(2-nitro-benzenesulfonyl)-amino]-but-2-enyl}-malonic acid dimethyl ester
Synonyms: 2-(4-Carboxy-benzyl)-2-{(Z)-4-[(6-hydroxy-hexyl)-(2-nitro-benzenesulfonyl)-amino]-but-2-enyl}-malonic acid dimethyl ester
CAS NO:292819-44-4
Molecular Formula:
Molecular Weight: 620.678
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: 2-(4-Carboxy-benzyl)-2-{(Z)-4-[(6-hydroxy-hexyl)-(2-nitro-benzenesulfonyl)-amino]-but-2-enyl}-malonic acid dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-Carboxy-benzyl)-2-{(Z)-4-[(6-hydroxy-hexyl)-(2-nitro-benzenesulfonyl)-amino]-but-2-enyl}-malonic acid dimethyl ester(292819-44-4)
EPA Substance Registry System: 2-(4-Carboxy-benzyl)-2-{(Z)-4-[(6-hydroxy-hexyl)-(2-nitro-benzenesulfonyl)-amino]-but-2-enyl}-malonic acid dimethyl ester(292819-44-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 292819-44-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 292819-44-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,2,8,1 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 292819-44:
(8*2)+(7*9)+(6*2)+(5*8)+(4*1)+(3*9)+(2*4)+(1*4)=174
174 % 10 = 4
So 292819-44-4 is a valid CAS Registry Number.

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292819-44-4Relevant academic research and scientific papers

Solid-phase synthesis of hydroxy-acids leading to macrolactones

Gagnon, René,Dory, Yves L.,Deslongchamps, Pierre

, p. 4751 - 4755 (2007/10/03)

A sequence of five chemical steps on solid support yields hydroxy-acids in a very straightforward and efficient manner. The resulting compounds can be cyclized in solution phase by forming an ester bond to produce macrolactones. (C) 2000 Published by Elsevier Science Ltd.

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