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1222106-45-7

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1222106-45-7 Usage

Uses

7-Benzyl-4,7-diaza-spiro[2.5]octane is a useful research chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 1222106-45-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,2,1,0 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1222106-45:
(9*1)+(8*2)+(7*2)+(6*2)+(5*1)+(4*0)+(3*6)+(2*4)+(1*5)=87
87 % 10 = 7
So 1222106-45-7 is a valid CAS Registry Number.

1222106-45-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-benzyl-4,7-diazaspiro[2.5]octane

1.2 Other means of identification

Product number -
Other names -

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:1222106-45-7 SDS

1222106-45-7Relevant articles and documents

Synthesis method of 4,7-diazaspiro[2.5]octane compound

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Paragraph 0081-0087, (2020/11/26)

The invention discloses a synthesis method of a 4,7-diazaspiro[2.5]octane compound, which comprises the following steps: by using a derivative of 4-methoxybenzyl-(1-(hydroxymethyl) cyclopropyl) carbamate as a raw material, substituting, adding a protecting group, removing the protecting group, and performing reduction to obtain the 4,7-diazaspiro[2.5]octane compound. According to the method disclosed by the invention, a flammable and combustible boron trifluoride diethyl ether adduct with corrosive toxicity is prevented from being used in a synthesis route to carry out a synthesis reaction, and the safety in the synthesis reaction is improved.

Preparation method of 4,7-diazaspiro[2.5]octane derivative

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, (2018/12/13)

The invention provides a preparation method of 4,7-diazaspiro[2.5]octane derivative. The 4,7-diazaspiro[2.5]octane derivative is prepared by taking 1-aminocyclopropane carboxylate as a starting material. The preparation method has the advantages of simple operation steps, stable process conditions, high controllability, high product yield (the four-step reaction yield of compounds shown as formulas II to I can be up to 70 percent), environmental friendliness and the like, and is suitable for large-scale production.

IMIDAZOTHIAZOLE DERIVATIVE HAVING PROLINE RING STRUCTURE

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, (2011/11/07)

[Problem to be Solved] There is provided a novel compound that inhibits interaction between murine double minute 2 (Mdm2) protein and p53 protein and exhibits anti-tumor activity. [Solution] The present invention provides an imidazothiazole derivative rep

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