Cas 1243660-23-2,methyl 3-(diethoxyphosphoryl)-5-n-hexyl-6-hydroxy-2-methylbenzoate

1243660-23-2

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Basic information

Product Name: methyl 3-(diethoxyphosphoryl)-5-n-hexyl-6-hydroxy-2-methylbenzoate
Synonyms: methyl 3-(diethoxyphosphoryl)-5-n-hexyl-6-hydroxy-2-methylbenzoate
CAS NO:1243660-23-2
Molecular Formula:
Molecular Weight: 386.425
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: methyl 3-(diethoxyphosphoryl)-5-n-hexyl-6-hydroxy-2-methylbenzoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 3-(diethoxyphosphoryl)-5-n-hexyl-6-hydroxy-2-methylbenzoate(1243660-23-2)
EPA Substance Registry System: methyl 3-(diethoxyphosphoryl)-5-n-hexyl-6-hydroxy-2-methylbenzoate(1243660-23-2)

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: 1243660-23-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1243660-23-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,3,6,6 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1243660-23:
(9*1)+(8*2)+(7*4)+(6*3)+(5*6)+(4*6)+(3*0)+(2*2)+(1*3)=132
132 % 10 = 2
So 1243660-23-2 is a valid CAS Registry Number.

1243660-23-2Upstream product

1031694-89-9 1-methoxy-1,3-bis(trimethylsilyloxy)deca-1,3-diene

1243660-23-2Downstream Products

1243660-23-2Relevant academic research and scientific papers

Regioselective Synthesis of Highly Functionalized Arylphosphonates by Cyclocondensation of 1,3-Bis(trimethylsilyloxy)buta-1,3-dienes with 3-Ethoxy-2-phosphonylalk-2-en-1-ones

Fatunsin, Olumide,Shkoor, Mohanad,Riahi, Abdolmajid,Langer, Peter

experimental part, p. 1525 - 1527 (2010/08/20)

Highly functionalized arylphosphonates were prepared by TiCl 4-mediated cyclocondensation of 3-ethoxy-2-phosphonylalk-2-en-1-ones with 1,3-bis(trimethylsilyloxy)buta-1,3-dienes. Georg Thieme Verlag Stuttgart New York.

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