Cas 1369950-37-7,4-(4-hydroxybenzyl)-2-methyl-5-oxo-2-propyl-2,5-dihydrooxazole 3-oxide

1369950-37-7

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Basic information

Product Name: 4-(4-hydroxybenzyl)-2-methyl-5-oxo-2-propyl-2,5-dihydrooxazole 3-oxide
Synonyms: 4-(4-hydroxybenzyl)-2-methyl-5-oxo-2-propyl-2,5-dihydrooxazole 3-oxide
CAS NO:1369950-37-7
Molecular Formula:
Molecular Weight: 263.293
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: 4-(4-hydroxybenzyl)-2-methyl-5-oxo-2-propyl-2,5-dihydrooxazole 3-oxide(CAS DataBase Reference)
NIST Chemistry Reference: 4-(4-hydroxybenzyl)-2-methyl-5-oxo-2-propyl-2,5-dihydrooxazole 3-oxide(1369950-37-7)
EPA Substance Registry System: 4-(4-hydroxybenzyl)-2-methyl-5-oxo-2-propyl-2,5-dihydrooxazole 3-oxide(1369950-37-7)

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: 1369950-37-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1369950-37-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,9,9,5 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1369950-37:
(9*1)+(8*3)+(7*6)+(6*9)+(5*9)+(4*5)+(3*0)+(2*3)+(1*7)=207
207 % 10 = 7
So 1369950-37-7 is a valid CAS Registry Number.

1369950-37-7Upstream product

107-87-9 2-Pentanone

1369950-37-7Downstream Products

1369950-37-7Relevant academic research and scientific papers

Nitrone formation in phosphate buffer and aqueous solutions: Novel chemistry inspired by a natural product

Pansanit, Acharavadee,Ingavat, Nattha,Aree, Thammarat,Mahidol, Chulabhorn,Ruchirawat, Somsak,Kittakoop, Prasat

, p. 2129 - 2131 (2012)

Nitrones are formed from the reaction of aspergillusol A (1) and a ketone/aldehyde in phosphate buffer and aqueous solutions with pH ranges of 6.8-8.6, resembling physiological conditions. The reaction of 1 with 1-substituted cyclohexanones gave the (1′S,2′R)-isomer, diastereoselectively.

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