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CAS

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1008097-01-5

3-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-4'-methoxy-1,1'-biphenyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1008097-01-5 Structure

  • Basic information

    1. Product Name: 3-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-4'-methoxy-1,1'-biphenyl
    2. Synonyms: 3-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-4'-methoxy-1,1'-biphenyl
    3. CAS NO:1008097-01-5
    4. Molecular Formula:
    5. Molecular Weight: 350.228
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1008097-01-5.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: 3-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-4'-methoxy-1,1'-biphenyl(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-4'-methoxy-1,1'-biphenyl(1008097-01-5)
    11. EPA Substance Registry System: 3-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-4'-methoxy-1,1'-biphenyl(1008097-01-5)

  • 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: 1008097-01-5(Hazardous Substances Data)

1008097-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1008097-01-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,8,0,9 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1008097-01:
(9*1)+(8*0)+(7*0)+(6*8)+(5*0)+(4*9)+(3*7)+(2*0)+(1*1)=115
115 % 10 = 5
So 1008097-01-5 is a valid CAS Registry Number.

1008097-01-5Downstream Products

1008097-01-5Relevant articles and documents

Direct transformation from arylamines to aryl naphthalene-1,8-diamino boronamides: A metal-free sandmeyer-type process

Ding, Siyi,Ma, Qiang,Zhu, Min,Ren, Huaping,Tian, Shaopeng,Zhao, Yuzhen,Miao, Zongcheng

, (2019)

A direct metal-free transformation from arylamines to aryl naphthalene-1,8-diamino boronamides, a type of masked boronic acid, has been developed based on Sandmeyer-type reactions. A nonsymmetrical diboron reagent, B(pin)-B(dan), was utilized as the boryl

Differentially protected benzenediboronic acids: Divalent cross-coupling modules for the efficient synthesis of boron-substituted oligoarenes

Noguchi, Hiroyoshi,Shioda, Takayuki,Chou, Chih-Ming,Suginome, Michinori

, p. 377 - 380 (2008/09/19)

On the basis of the boron-masking strategy, new divalent cross-coupling modules have been designed for the efficient synthesis of boronsubstituted oligoarenes. The modules, i.e., monoprotected o-, m-, and p-benzenediboronic acid derivatives, undergo highly selective SuzukiMiyaura coupling with sp 2 iodides, bromides, chlorides, and triflates, affording coupling products in which the protected boronyl groups are left intact.

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