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1644382-35-3

C11H15N is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1644382-35-3 Structure

  • Basic information

    1. Product Name: C11H15N
    2. Synonyms: C11H15N
    3. CAS NO:1644382-35-3
    4. Molecular Formula:
    5. Molecular Weight: 161.247
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1644382-35-3.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: C11H15N(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H15N(1644382-35-3)
    11. EPA Substance Registry System: C11H15N(1644382-35-3)

  • 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: 1644382-35-3(Hazardous Substances Data)

1644382-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1644382-35-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,4,4,3,8 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1644382-35:
(9*1)+(8*6)+(7*4)+(6*4)+(5*3)+(4*8)+(3*2)+(2*3)+(1*5)=173
173 % 10 = 3
So 1644382-35-3 is a valid CAS Registry Number.

1644382-35-3Relevant articles and documents

Palladium(II)-catalyzed intramolecular tandem aminoalkylation via divergent C(sp3)-H functionalization

Du, Wei,Gu, Qiangshuai,Li, Zhongliang,Yang, Dan

supporting information, p. 1130 - 1135 (2015/02/05)

(Chemical Equation Presented) We have developed a Pd(II)-catalyzed oxidative tandem aminoalkylation via divergent C(sp3)-H functionalization, a ffording three- and five-membered-ring fused indolines in good yields under two optimized conditions, respectively. The mechanism studies have indicated that the benzylic C - H cleavage involved in the former transformation is the rate-determining step, while the cleavage of amide α-C - H in the latter is not. This is the first example of a Pd-catalyzed tandem reaction involving C(sp3)-H activation without the employment of prefunctionalized reagents (e.g., halogenated and boron reagents) and directing groups, representing a green and economic protocol for the construction of N-containing heterocycles.

Intramolecular aminocyanation of alkenes by N-CN bond cleavage

Pan, Zhongda,Pound, Sarah M.,Rondla, Naveen R.,Douglas, Christopher J.

, p. 5170 - 5174 (2014/05/20)

A metal-free, Lewis acid promoted intramolecular aminocyanation of alkenes was developed. B(C6F5)3 activates N-sulfonyl cyanamides, thus leading to a formal cleavage of the N-CN bonds in conjunction with vicinal addition o

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