161330-30-9

• 

• Basic information

  1. Product Name: 2-FLUOROPHENYLGLYCINE-N-BOC PROTECTED
  2. Synonyms: N-BOC-2-FLUOROPHENYLGLYCINE;2-Fluoro-DL-phenylglycine, N-BOC protected;a-(Boc-amino)-2-fluorobenzeneacetic acid;N-Boc-DL-2-FluoroPhenylglycine
  3. CAS NO:161330-30-9
  4. Molecular Formula: C₁₃H₁₆FNO₄
  5. Molecular Weight: 269.2704
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 161330-30-9.mol
  9. Article Data: 11

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 403.5°C at 760 mmHg
  3. Flash Point: 197.8°C
  4. Appearance: /
  5. Density: 1.242g/cm³
  6. Vapor Pressure: 3.1E-07mmHg at 25°C
  7. Refractive Index: 1.519
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. PKA: 3.23±0.10(Predicted)
  11. CAS DataBase Reference: 2-FLUOROPHENYLGLYCINE-N-BOC PROTECTED(CAS DataBase Reference)
  12. NIST Chemistry Reference: 2-FLUOROPHENYLGLYCINE-N-BOC PROTECTED(161330-30-9)
  13. EPA Substance Registry System: 2-FLUOROPHENYLGLYCINE-N-BOC PROTECTED(161330-30-9)

• Safety Data

  1. Hazard Codes: Xi
  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: 161330-30-9(Hazardous Substances Data)

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• SDS
• Upstream product
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161330-30-9 Suppliers

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• 2-((tert-Butoxycarbonyl)amino)-2-(2-fluorophenyl)acetic acid

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• Benzeneacetic acid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-2-fluoro-

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• Benzeneacetic acid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-2-fluoro- 161330-30-9

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• 2-((tert-Butoxycarbonyl)amino)-2-(2-fluorophenyl)acetic acid

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• HANGZHOU TIANYE CHEMICALS CO., LTD.
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• 2-(2-fluorophenyl)-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]acetic acid

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• N-Boc-DL-2-FluoroPhenylglycine161330-30-9

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• N-Boc-DL-2-FluoroPhenylglycine

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• Shanghai Apeptide Co., Ltd.
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161330-30-9 Usage

General Description

2-Fluorophenylglycine-N-Boc protected is a chemical compound that is commonly used in the synthesis of pharmaceuticals and other organic compounds. It is a derivative of glycine, an important amino acid, and features a Boc (tert-butyloxycarbonyl) protecting group to shield the amine functionality. The fluorine atom on the phenyl ring adds unique reactivity to the molecule, making it a valuable building block for the creation of various complex organic compounds. 2-FLUOROPHENYLGLYCINE-N-BOC PROTECTED is commonly used in the pharmaceutical industry for the development of new drugs and is also utilized in academic research for the study of organic chemistry and chemical reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 161330-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,3,3 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 161330-30:
(8*1)+(7*6)+(6*1)+(5*3)+(4*3)+(3*0)+(2*3)+(1*0)=89
89 % 10 = 9
So 161330-30-9 is a valid CAS Registry Number.

InChI:InChI=1/C13H16FNO4/c1-13(2,3)19-12(18)15-10(11(16)17)8-6-4-5-7-9(8)14/h4-7,10H,1-3H3,(H,15,18)(H,16,17)

161330-30-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-(2-fluorophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid

1.2 Other means of identification

Product number	-
Other names	[(tert-butoxycarbonyl)amino](2-fluorophenyl)acetic acid

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:161330-30-9 SDS

161330-30-9Upstream product

• 124-38-9 carbon dioxide 
• 1174761-19-3 N-(tert-butoxycarbonyl)-α-(phenylsulfonyl)-2-fluorobenzylamine 
• 446-52-6 2-Fluorobenzaldehyde 
• 24424-99-5 di-tert-butyl dicarbonate 
• 84145-28-8 (+/-)-2-amino-2'-fluorophenylacetic acid 
• 1358791-63-5 N-(tert-butoxycarbonyl)-α-(tributylstannyl)-2-fluorobenzylamine 

161330-30-9Downstream Products

• 709665-72-5 methyl 2-((tert-butoxycarbonyl)amino)-2-(2-fluorophenyl)acetate 
• 1379513-73-1 (3R)-3-(2-(tert-butoxycarbonylamino)-2-(2-fluorophenyl)acetoxy)-1-(2-oxo-2-phenylethyl)-1-azoniabicyclo[2.2.2]octane bromide 
• 1379513-72-0 (R)-quinuclidin-3-yl 2-(tert-butoxycarbonylamino)-2-(2-fluorophenyl)acetate 

161330-30-9Relevant articles and documents

Synthesis ofN-Boc-α-amino Acids from Carbon Dioxide by Electrochemical Carboxylation ofN-Boc-α-aminosulfones

Senboku, Hisanori,Minemura, Yoshihito,Suzuki, Yuto,Matsuno, Hidetoshi,Takakuwa, Mayu

, p. 16077 - 16083 (2021/10/12)

Electrochemical reduction ofN-Boc-α-aminosulfones in DMF using an undivided cell equipped with a Pt plate cathode and an Mg rod anode under atmospheric pressure of bubbling carbon dioxide through the solution under constant current conditions resulted in a reductive C-S bond cleavage with elimination of benzenesulfinate ion generating the corresponding anion species followed by fixation of carbon dioxide to give the correspondingN-Boc-α-amino acids in moderate to good yields.

HETEROARYL DERIVATIVES

-

Paragraph 0502; 0503; 0504; 0505, (2015/06/17)

Compounds of formula (I) described herein are both phosphodiesterase 4 (PDE4) enzyme inhibitors and muscarinic M3 receptor antagonists and are useful for the prevention and/or treatment of diseases of the respiratory tract characterized by airway obstruction.

PHENYLETHYLPYRIDINE DERIVATIVES AS PDE4-INHIBITORS

-

Page/Page column 69; 70, (2014/06/24)

The invention relates to novel compounds which are both inhibitors of the phosphodiesterase 4 (PDE4) enzyme and muscarinic M3 receptor antagonists, methods of preparing such compounds, compositions containing them and therapeutic use thereof.

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