Cas 1180657-24-2,1-(4-methylphenoxy)-3-({4-[(4-methylphenoxy)methyl]-3-nitrothiophen-2-yl}thio)propan-2-one

1180657-24-2

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Basic information

Product Name: 1-(4-methylphenoxy)-3-({4-[(4-methylphenoxy)methyl]-3-nitrothiophen-2-yl}thio)propan-2-one
Synonyms: 1-(4-methylphenoxy)-3-({4-[(4-methylphenoxy)methyl]-3-nitrothiophen-2-yl}thio)propan-2-one
CAS NO:1180657-24-2
Molecular Formula:
Molecular Weight: 443.544
EINECS: N/A
Product Categories: N/A
Mol File: 1180657-24-2.mol
Article Data: 1

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: 1-(4-methylphenoxy)-3-({4-[(4-methylphenoxy)methyl]-3-nitrothiophen-2-yl}thio)propan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-methylphenoxy)-3-({4-[(4-methylphenoxy)methyl]-3-nitrothiophen-2-yl}thio)propan-2-one(1180657-24-2)
EPA Substance Registry System: 1-(4-methylphenoxy)-3-({4-[(4-methylphenoxy)methyl]-3-nitrothiophen-2-yl}thio)propan-2-one(1180657-24-2)

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: 1180657-24-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1180657-24-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,0,6,5 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1180657-24:
(9*1)+(8*1)+(7*8)+(6*0)+(5*6)+(4*5)+(3*7)+(2*2)+(1*4)=152
152 % 10 = 2
So 1180657-24-2 is a valid CAS Registry Number.

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1180657-24-2Relevant articles and documents

Nitroketene dithioacetal chemistry: Synthesis of 2-alkylthio-3- nitrothiophenes from nitroketene dithioacetate and chloromethyl ketones

Surya Prakash Rao,Vasantham

supporting information; experimental part, p. 6847 - 6850 (2009/12/31)

(Chemical Equation Presented) An effective synthesis of highly functionalized 3-nitrothiophenes was achieved from the reaction of simple, inexpensive, and readily available dipotassium 2-nitro-1, 1-ethylyenedithiolate with α-chloromethyl ketones in toluen

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