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1-Boc-3-(bromomethyl)azetidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

253176-93-1

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253176-93-1 Usage

Uses

It is used as an active pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 253176-93-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,1,7 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 253176-93:
(8*2)+(7*5)+(6*3)+(5*1)+(4*7)+(3*6)+(2*9)+(1*3)=141
141 % 10 = 1
So 253176-93-1 is a valid CAS Registry Number.

253176-93-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H57492)  1-Boc-3-(bromomethyl)azetidine, 95%   

  • 253176-93-1

  • 250mg

  • 1435.0CNY

  • Detail
  • Alfa Aesar

  • (H57492)  1-Boc-3-(bromomethyl)azetidine, 95%   

  • 253176-93-1

  • 500mg

  • 2393.0CNY

  • Detail

253176-93-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 3-(bromomethyl)azetidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names N-(TERT-BUTOXYCARBONYL)-3-BROMOMETHYLAZETIDINE

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:253176-93-1 SDS

253176-93-1Relevant academic research and scientific papers

REDUCTION OF PRO-INFLAMMATORY HDL USING A LEUKOTRIENE INHIBITOR

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, (2018/09/12)

A method involving the administration of a therapeutically effective amount of a leukotriene inhibitor, a pharmaceutically acceptable salt, a pharmaceutically acceptable N-oxide, a pharmaceutically active metabolite, a pharmaceutically acceptable prodrug, or pharmaceutically acceptable solvate thereof to a human for reducing a level of pro-inflammatory HDL in the human. Various examples of leukotriene inhibitors, including 3-[3-tert-butylsulfanyl-1-[4-(6-ethoxy-pyridin- 3-yl)-benzyl]-5-(5-methyl-pyridin-2-ylmethoxy)-1H-indol-2-yl]-2, 2-dimethyl-propionic acid, are disclosed for administration for the reduction of pro-inflammatory HDL in a human. Reduction of pro-inflammatory HDL by the leukotriene inhibitor may include conversion of at least a portion of pro-inflammatory HDL to anti-inflammatory HDL.

5-LIPOXYGENASE-ACTIVATING PROTEIN (FLAP) INHIBITORS

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Page/Page column 63, (2008/06/13)

Described herein are compounds and pharmaceutical compositions containing such compounds, which modulate the activity of 5-lipoxygenase-activating protein (FLAP). Also described herein are methods of using such FLAP modulators, alone and in combination with other compounds, for treating respiratory, cardiovascular, and other leukotriene-dependent or leukotriene mediated conditions or diseases.

CHK-1 INHIBITORS

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Page/Page column 220, (2010/02/11)

Disclosed are novel inhibitors of Chk-1 and methods of using the same for therapy.

Beta lactam compounds and their use as inhibitors of tryptase

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Page column 207, (2010/11/29)

Compounds of the formulas: are disclosed. These compounds inhibit tryptase as well as other enzyme systems or are selective tryptase inhibitors and are useful as antiinflammatory agents particularly in the treatment of chronic asthma.

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