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1155843-79-0

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1155843-79-0 Usage

Uses

2-Hydroxy-2-azaadamantane is a catalysis for the efficient C(sp3)-H bond functionalization of Isochroman.

Check Digit Verification of cas no

The CAS Registry Mumber 1155843-79-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,5,8,4 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1155843-79:
(9*1)+(8*1)+(7*5)+(6*5)+(5*8)+(4*4)+(3*3)+(2*7)+(1*9)=170
170 % 10 = 0
So 1155843-79-0 is a valid CAS Registry Number.

1155843-79-0 Well-known Company Product Price

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  • (Code)Product description
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  • Detail
  • TCI America

  • (H1404)  2-Hydroxy-2-azaadamantane  >98.0%(GC)(T)

  • 1155843-79-0

  • 200mg

  • 390.00CNY

  • Detail
  • TCI America

  • (H1404)  2-Hydroxy-2-azaadamantane  >98.0%(GC)(T)

  • 1155843-79-0

  • 1g

  • 1,180.00CNY

  • Detail
  • TCI America

  • (H1404)  2-Hydroxy-2-azaadamantane  >98.0%(GC)(T)

  • 1155843-79-0

  • 5g

  • 3,980.00CNY

  • Detail

1155843-79-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Hydroxy-2-azaadamantane

1.2 Other means of identification

Product number -
Other names AZADOL(R)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1155843-79-0 SDS

1155843-79-0Relevant articles and documents

Oxidative conversion of silyl enol ethers to α,β-unsaturated ketones employing oxoammonium salts

Hayashi, Masaki,Shibuya, Masatoshi,Iwabuchi, Yoshiharu

supporting information; scheme or table, p. 154 - 157 (2012/02/16)

The oxidative conversion of silyl enol ethers to α,β-unsaturated ketones using a less-hindered class of oxoammonium salts (AZADO +BF4-) is described. The reaction proceeds via the ene-like addition of oxoammonium salts to silyl enol ethers.

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