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2-Methoxy-6-vinyl-1-nitrobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 150330-40-8 Structure
  • Basic information

    1. Product Name: 2-Methoxy-6-vinyl-1-nitrobenzene
    2. Synonyms: 2-Methoxy-6-vinyl-1-nitrobenzene
    3. CAS NO:150330-40-8
    4. Molecular Formula:
    5. Molecular Weight: 179.175
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 150330-40-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Methoxy-6-vinyl-1-nitrobenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Methoxy-6-vinyl-1-nitrobenzene(150330-40-8)
    11. EPA Substance Registry System: 2-Methoxy-6-vinyl-1-nitrobenzene(150330-40-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 150330-40-8(Hazardous Substances Data)

150330-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150330-40-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,3,3 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 150330-40:
(8*1)+(7*5)+(6*0)+(5*3)+(4*3)+(3*0)+(2*4)+(1*0)=78
78 % 10 = 8
So 150330-40-8 is a valid CAS Registry Number.

150330-40-8Relevant articles and documents

Benzazaborinines as novel bioisosteric replacements of naphthalene: Propranolol as an example

Rombouts, Frederik J. R.,Tovar, Fulgencio,Austin, Nigel,Tresadern, Gary,Trabanco, Andrés A.

, p. 9287 - 9295 (2015)

Two benzazaborinine analogues of propranolol were synthesized and extensively profiled in vitro and in vivo. These analogues showed potency and physicochemical and in vitro ADME-tox profiles comparable to propranolol. In addition, both benzazaborinine ana

Development of isomerization and cycloisomerization with use of a ruthenium hydride with N-heterocyclic carbene and its application to the synthesis of heterocycles

Arisawa, Mitsuhiro,Terada, Yukiyoshi,Takahashi, Kazuyuki,Nakagawa, Masako,Nishida, Atsushi

, p. 4255 - 4261 (2007/10/03)

A pure ruthenium hydride complex with N-heterocyclic carbene (NHC) ligand was efficiently generated from the reaction of a second-generation Grubbs ruthenium catalyst with vinyloxytrimethylsilane and unambiguously characterized. This ruthenium hydride complex showed high catalytic activity for the selective isomerization of terminal olefin and for the cycloisomerization of 1,6-dienes. These reactions of N-allyl-o-vinylaniline lead to novel synthetic methods for heterocycles such as indoles and 3-methylene-2,3-dihydroindoles, which are useful synthons for bioactive natural products. These procedures address an important issue in diversity-oriented synthesis.

TRICYCLIC HETEROCYCLIC COMPOUND

-

, (2008/06/13)

Tricyclic heterocyclyl compounds having a general formula (I): wherein: R1 and R2 each represents H, a lower alkyl or lower alkoxy group, a halogen atom or halogeno-lower alkyl; R3 represents H or a lower alkyl group; R4 represents a substituted phenyl or

Structure-activity relationship of a series of phenylureas linked to 4- phenylimidazole. Novel potent inhibitors of acyl-CoA:cholesterol O- acyltransferase with antiatherosclerotic activity. 2

Kimura,Watanabe,Matsui,Hayashi,Tanaka,Ohtsuka,Saeki,Kogushi,Kabayashi,Akasaka,Yamagishi,Saitou,Yamatsu

, p. 1641 - 1653 (2007/10/02)

In our continuing search to find systemically bioavailable ACAT (acyl- CoA:cholesterol O-acyl-transferase) inhibitors with more potent antiatherosclerotic effect than N-[2-(dimethylamino)-6-[3-(5-methyl-4- phenyl-1H-imidazol-1-yl)propoxy]phenyl]-N'-pentyl

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