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3-Methyl-1,6-heptadiene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 50871-05-1 Structure
  • Basic information

    1. Product Name: 3-Methyl-1,6-heptadiene
    2. Synonyms: 3-Methyl-1,6-heptadiene
    3. CAS NO:50871-05-1
    4. Molecular Formula: C8H14
    5. Molecular Weight: 110.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 50871-05-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-Methyl-1,6-heptadiene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Methyl-1,6-heptadiene(50871-05-1)
    11. EPA Substance Registry System: 3-Methyl-1,6-heptadiene(50871-05-1)
  • 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: 50871-05-1(Hazardous Substances Data)

50871-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50871-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,7 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 50871-05:
(7*5)+(6*0)+(5*8)+(4*7)+(3*1)+(2*0)+(1*5)=111
111 % 10 = 1
So 50871-05-1 is a valid CAS Registry Number.

50871-05-1Downstream Products

50871-05-1Relevant articles and documents

1,4-CYCLOHEPTYLENE AND THE RELATED ALLYLIC DIRADICALS. THERMAL NITROGEN EXTRUSION FROM 6,7-DIAZABICYCLONON-6-ENES

Uyehara, Tadao,Takahashi, Masayuki,Kato, Tadahiro

, p. 1241 - 1244 (2007/10/02)

Thermal nitrogen extrusion of 2-methylene-6,7-diazabicyclonon-6-enes and 6,7-diazabicyclonona-2,6-dienes proceeded easily to give closure and cleavage products via the corresponding 5-methylene-1,4-cycloheptylenes and 4-cyclohepten-1,3-ylenes, respectively.

(Alkenyl-η3-allyl)bis(η5-cyclopentadienyl)titanium Complexes

Lehmkuhl, Herbert,Fustero, Santos

, p. 1353 - 1360 (2007/10/02)

Bis(η5-cyclopentadienyl)titanium hydride (Cp2TiH), presumably formed in situ from bis(η5-cyclopentadienyl)titanium dichloride (1) and isopropylmagnesium bromide (2) adds to the conjugated C=C bonds of the alkatrienes 4, 5, 25, 36, and 45 to give the (alkenyl-η3-allyl)bis(η5-cyclopentadienyl)titanium complexes 7 and 10, 8, 26, and 30, 37, 46.The complexes 7, 8, and 26 with the alkenyl group in position 1 isomerize to give the compounds 27, 28, and 29 in which the C=C bond is conjugated with the allyl group.Compound 37 which contains an alkenyl group in a meso-position does not isomerize.In the case of isomycoren (40), TiH addition occurs primarily to the isolated C=C bond followed by intramolecular cyclization to give the bis(η5-cyclopentadienyl)(1-cyclopentyl-η3-allyl)titanium complex 41.

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