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185456-26-2

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185456-26-2 Usage

General Description

BOC3-HYDRAZINE is a compound that consists of a hydrazine molecule (N2H4) attached to a tert-butyloxycarbonyl (BOC) protective group. It is commonly used as a reagent in organic synthesis and as a building block for the preparation of various pharmaceuticals and agrochemicals. BOC3-HYDRAZINE is also utilized in the manufacturing of polymer crosslinkers, dyes, and as a chemical intermediate. It is a stable and versatile compound that has found applications in a wide range of industries due to its ability to release hydrazine under specific reaction conditions. However, it is important to handle BOC3-HYDRAZINE with caution due to its potential toxicity and flammability.

Check Digit Verification of cas no

The CAS Registry Mumber 185456-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,4,5 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 185456-26:
(8*1)+(7*8)+(6*5)+(5*4)+(4*5)+(3*6)+(2*2)+(1*6)=162
162 % 10 = 2
So 185456-26-2 is a valid CAS Registry Number.

185456-26-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[(2-methylpropan-2-yl)oxycarbonyl]-N-[(2-methylpropan-2-yl)oxycarbonylamino]carbamate

1.2 Other means of identification

Product number -
Other names 1,1,2-Boc3-hydrazine

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:185456-26-2 SDS

185456-26-2Relevant articles and documents

Addition of arylboronic acids to symmetrical and unsymmetrical azo compounds

Kisseljova, Ksenija,Tsubrik, Olga,Sillard, Rannar,Maeeorg, Sirje,Maeeorg, Uno

, p. 43 - 45 (2007/10/03)

(Chemical Equation Presented) The addition of aryl- and heteroarylboronic acids to azo compounds is described. Copper salt catalysis was necessary to perform the reaction under mild conditions and high yields. Excellent regioselectivity was observed in addition to unsymmetrical azo compounds.

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