162045-48-9

• 

• Basic information

  1. Product Name: 1-BOC-4-[(2-HYDROXYPHENYL)AMINO]-PIPERIDINE
  2. Synonyms: 1-BOC-4-[(2-HYDROXYPHENYL)AMINO]-PIPERIDINE;tert-Butyl 4-((2-hydroxyphenyl)aMino)piperidine-1-carboxylate
  3. CAS NO:162045-48-9
  4. Molecular Formula: C₁₆H₂₄N₂O₃
  5. Molecular Weight: 292.377
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 162045-48-9.mol
  9. Article Data: 10

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 429.801°C at 760 mmHg
  3. Flash Point: 213.736°C
  4. Appearance: /
  5. Density: 1.179g/cm³
  6. Vapor Pressure: 0mmHg at 25°C
  7. Refractive Index: 1.58
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 1-BOC-4-[(2-HYDROXYPHENYL)AMINO]-PIPERIDINE(CAS DataBase Reference)
  11. NIST Chemistry Reference: 1-BOC-4-[(2-HYDROXYPHENYL)AMINO]-PIPERIDINE(162045-48-9)
  12. EPA Substance Registry System: 1-BOC-4-[(2-HYDROXYPHENYL)AMINO]-PIPERIDINE(162045-48-9)

• 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: 162045-48-9(Hazardous Substances Data)

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• 1-BOC-4-(2-HYDROXYPHENYLAMINO)PIPERIDINE

  Cas No: 162045-48-9

• USD $ 3.0-3.0 / Kilogram

• 1 Kilogram

• 1-100 Metric Ton/Month

• Dayang Chem (Hangzhou) Co.,Ltd.
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• 1-Piperidinecarboxylicacid, 4-[(2-hydroxyphenyl)amino]-, 1,1-dimethylethyl ester

  Cas No: 162045-48-9

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• Hangzhou J&H Chemical Co., Ltd.
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• 1-BOC-4-[(2-HYDROXYPHENYL)AMINO]-PIPERIDINE

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• ZHEJIANG JIUZHOU CHEM CO.,LTD
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• 1-BOC-4-[(2-HYDROXYPHENYL)AMINO]-PIPERIDINE

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• Finetech Industry Limited
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• tert-Butyl 4-((2-hydroxyphenyl)amino)piperidine-1-carboxylate

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• ENAO Chemical Co, Limited
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• 1-Boc-4-[(2-hydroxyphenyl)amino]piperidine

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162045-48-9 Usage

General Description

1-BOC-4-[(2-HYDROXYPHENYL)AMINO]-PIPERIDINE is a compound that consists of a piperidine ring with a 2-hydroxyphenylamino group attached to the 4-position. The BOC group is a protecting group often used in organic synthesis to protect amines from unwanted reactions. 1-BOC-4-[(2-HYDROXYPHENYL)AMINO]-PIPERIDINE may have potential applications in the pharmaceutical industry, particularly in the synthesis of new drug candidates. The 2-hydroxyphenylamino group suggests potential biological activity, as phenolic compounds are known to exhibit antioxidant and anti-inflammatory properties. The compound's structure could also make it suitable for incorporation into larger molecules or materials, making it a valuable building block for synthetic chemistry. Overall, 1-BOC-4-[(2-HYDROXYPHENYL)AMINO]-PIPERIDINE has potential utility in medicinal and materials chemistry, and further investigation into its properties and potential applications is warranted.

Check Digit Verification of cas no

The CAS Registry Mumber 162045-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,0,4 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 162045-48:
(8*1)+(7*6)+(6*2)+(5*0)+(4*4)+(3*5)+(2*4)+(1*8)=109
109 % 10 = 9
So 162045-48-9 is a valid CAS Registry Number.

InChI:InChI=1/C16H24N2O3/c1-16(2,3)21-15(20)18-10-8-12(9-11-18)17-13-6-4-5-7-14(13)19/h4-7,12,17,19H,8-11H2,1-3H3

162045-48-9SDS

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 4-(2-hydroxyanilino)piperidine-1-carboxylate

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:162045-48-9 SDS

162045-48-9Upstream product

• 79099-07-3 N-tert-butyloxycarbonylpiperidin-4-one 
• 95-55-6 2-amino-phenol 
• 24424-99-5 di-tert-butyl dicarbonate 
• 40064-34-4 4-piperidone monohydrochloride monohydrate 
• 107-06-2 1,2-dichloro-ethane 

162045-48-9Downstream Products

• 215878-20-9 4-[2(3H)-oxobenzoxazol-3-yl]piperidine 
• 1023289-11-3 2-(piperidin-4-ylamino)-phenol hydrochloride 
• 162045-49-0 4-(2-Ethoxycarbonylmethoxy-phenylamino)-piperidine-1-carboxylic acid tert-butyl ester 
• 356072-47-4 1-(Tert-Butoxycarbonyl)-4-[(2-methoxycarbonylmethoxyphenyl)amino]piperidine 
• 173842-04-1 5-Chloro-1,1-dioxido-2-(4-(4-(2-oxo-3-benzoxazolinyl)-piperidin-1-yl)-butyl)-1,2-benzisothiazol-3(2H)-one 
• 162045-53-6 tert-butyl-4-(2-oxobenzo[d]oxazole-3-(2H)-yl)piperidin-1-carboxylate 

162045-48-9Relevant articles and documents

DIPHENYLBUTYPIPERIDINE AUTOPHAGY INDUCERS

-

Page/Page column 7; 87-90, (2011/12/02)

Autophagy inducing compounds, methods of their preparation and use, and kits containg said compounds are disclosed herein.

Piperidine amides as 11β-hydroxysteroid dehydrogenase type 1 inhibitors

Flyrén, Katarina,Bergquist, Lars O.,Castro, Victor M.,Fotsch, Christopher,Johansson, Lars,St. Jean Jr., David J.,Sutin, Lori,Williams, Meredith

, p. 3421 - 3425 (2008/02/08)

A series of piperidine amide inhibitors of human 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) were identified via modifications of the HTS hit compound 1. The synthesis, in vitro biological evaluation, and structure-activity relationship of these co

Phenoxyalkylamine derivatives useful as opioid receptor agonists

-

, (2008/06/13)

A medicament useful for preventive and/or therapeutic treatment of nerve system diseases which comprises, as an active ingredient, a compound represented by the following general formula (I) or a pharmacologically acceptable salt thereof: wherein, X represents a group represented by the following general formula (II), (III), (IV), (V), or (VI), “A” represents a saturated or unsaturated 3- to 6-membered carbocyclic group and the like, “B” represents CH2 and the like, “n” represents 0 to 2, R1 represents a hydrogen atom, a halogen atom and the like, R2, R3, and R7 to R14 represent a hydrogen atom, a lower alkyl group which may be substituted and the like, R4 represents a hydrogen atom, a lower alkyl group which may be substituted and the like, R5 represents a hydrogen atom, a halogen atom and the like, R6 represents a saturated or unsaturated monocyclic or bicyclic carbocyclic group and the like, and R5 and R6, R7 and R8, R9 and R10, or R11 and R12 may bind to each other to form a cyclic structure.

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