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Bicyclo[2.2.1]heptane-2,5-diamine (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 171065-84-2 Structure
  • Basic information

    1. Product Name: Bicyclo[2.2.1]heptane-2,5-diamine (9CI)
    2. Synonyms: Bicyclo[2.2.1]heptane-2,5-diamine (9CI)
    3. CAS NO:171065-84-2
    4. Molecular Formula: C7H14N2
    5. Molecular Weight: 126.19946
    6. EINECS: N/A
    7. Product Categories: AMINEPRIMARY
    8. Mol File: 171065-84-2.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: Bicyclo[2.2.1]heptane-2,5-diamine (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Bicyclo[2.2.1]heptane-2,5-diamine (9CI)(171065-84-2)
    11. EPA Substance Registry System: Bicyclo[2.2.1]heptane-2,5-diamine (9CI)(171065-84-2)
  • 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: 171065-84-2(Hazardous Substances Data)

171065-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 171065-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,0,6 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 171065-84:
(8*1)+(7*7)+(6*1)+(5*0)+(4*6)+(3*5)+(2*8)+(1*4)=122
122 % 10 = 2
So 171065-84-2 is a valid CAS Registry Number.

171065-84-2Relevant articles and documents

A highly enantioselective catalyst for the asymmetric Nozaki-Hiyama-Kishi reaction of allylic and vinylic halides

Berkessel, Albrecht,Menche, Dirk,Sklorz, Christoph A.,Schroeder, Michael,Paterson, Ian

, p. 1032 - 1035 (2003)

Catalytic asymmetric addition of vinylic halides and trifiates to aldehydes, with useful levels of stereoinduction, has been achieved for the first time using the salentype ligand (S,S)-5 (see scheme; PMB=para-methoxybenzyl), which contains the novel endo

Novel polyisocyanate compound, method for producing the same, and uses thereof

-

Page/Page column 5, (2010/02/11)

The invention provides an optical material being excellent in balance between the heat resistance, Abbe number and refractive index by providing a compound represented by the general formula (1): in the formula, k and n representing integers of 0 to 2 and 0 to 1, respectively, with the proviso that k and n are not simultaneously zero, and k=0 meaning that —(CH2)k- is not included in the formula.

Enantioselective Synthesis of DIANANE, a Novel C2-Symmetric Chiral Diamine for Asymmetric Catalysis

Berkessel, Albrecht,Schroeder, Michael,Sklorz, Christoph A.,Tabanella, Stefania,Vogl, Nadine,Lex, Johann,Neudoerfl, Joerg M.

, p. 3050 - 3056 (2007/10/03)

DIANANE (endo,endo-2,5-diaminonorbornane) is a novel chiral C 2-symmetric diamine, based on the rigid bicyclo[2.2.1]heptane scaffold. Schiff-base ligands derived from DIANANE have already found use in asymmetric catalysis, e.g., in the highly e

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