126409-25-4

• 

• Basic information

  1. Product Name: 1-methylethyl [(1S,2S,4R)-1,4-dibenzyl-5-(benzylamino)-2-hydroxy-5-oxopentyl]carbamate
  2. Synonyms:
  3. CAS NO:126409-25-4
  4. Molecular Formula: C₃₁H₃₈N₂O₄
  5. Molecular Weight: 488.6178
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 126409-25-4.mol
  9. Article Data: 6

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 722.5°C at 760 mmHg
  3. Flash Point: 390.8°C
  4. Appearance: N/A
  5. Density: 1.147g/cm³
  6. Vapor Pressure: 6.54E-22mmHg at 25°C
  7. Refractive Index: 1.578
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 1-methylethyl [(1S,2S,4R)-1,4-dibenzyl-5-(benzylamino)-2-hydroxy-5-oxopentyl]carbamate(CAS DataBase Reference)
  11. NIST Chemistry Reference: 1-methylethyl [(1S,2S,4R)-1,4-dibenzyl-5-(benzylamino)-2-hydroxy-5-oxopentyl]carbamate(126409-25-4)
  12. EPA Substance Registry System: 1-methylethyl [(1S,2S,4R)-1,4-dibenzyl-5-(benzylamino)-2-hydroxy-5-oxopentyl]carbamate(126409-25-4)

• 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: 126409-25-4(Hazardous Substances Data)

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126409-25-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126409-25-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,4,0 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 126409-25:
(8*1)+(7*2)+(6*6)+(5*4)+(4*0)+(3*9)+(2*2)+(1*5)=114
114 % 10 = 4
So 126409-25-4 is a valid CAS Registry Number.

126409-25-4SDS

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	propan-2-yl N-[(2S,3S,5R)-5-benzyl-6-(benzylamino)-3-hydroxy-6-oxo-1-phenylhexan-2-yl]carbamate

1.2 Other means of identification

Product number	-
Other names	Boc-CH2Ph-NHBn deriv.

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:126409-25-4 SDS

126409-25-4Upstream product

• 38225-27-3 lithium benzylamide 
• 98818-41-8 (3R,5S)-3-benzyl-5-{(1S)-1-[(tert-butoxycarbonyl)amino]-2-phenylethyl}dihydrofuran-2-(3H)-one 
• 14131-84-1 2,3:5,6-di-O-isopropylidene-α-D-mannofuranose 
• 98818-45-2 5(S)-(Boc-amino)-4(S)-hydroxy-6-phenyl-2(R)-phenylmethylhexanoic acid 
• 137038-63-2 deux références: JFP452-1 et JFP456b 
• 137007-30-8 (R)-1-((S)-5-Methoxy-tetrahydro-furan-2-yl)-2-phenyl-ethanol 
• 137007-25-1 (R)-4-((S)-5-Methoxy-2,5-dihydro-furan-2-yl)-2,2-dimethyl-[1,3]dioxolane 
• 61845-17-8 methyl D-2,3-dideoxyglucofuranoside 
• 137007-28-4 (S)-2-Methoxy-5-(R)-oxiranyl-tetrahydro-furan 
• 68144-11-6 1,4-anhydro-2-deoxy-5,6-O-isopropylidene-D-arabinohex-1-enitol 
• 530-26-7 D-Mannose 
• 100-46-9 benzylamine 
• 143006-63-7 (4S,5S)-4-benzyl-3-(tert-butoxycarbonyl)-5-((2R)-3-hydroxy-2-benzylpropyl)-2,2-dimethyl-1,3-oxazolidine 
• 143006-64-8 (4S,5S)-4-benzyl-3-(tert-butoxycarbonyl)-5-((2R)-2-carboxy-3-phenylpropyl)-2,2-dimethyl-1,3-oxazolidine 

126409-25-4Downstream Products

126409-25-4Relevant articles and documents

Ring-closing metathesis strategy to unsaturated γ- and δ-lactones: Synthesis of hydroxyethylene isostere for protease inhibitors

Ghosh, Arun K.,Cappiello, John,Shin, Dongwoo

, p. 4651 - 4654 (2007/10/03)

Ring-closing olefin metathesis of acrylates derived from allylic and homo allylic alcohols in the presence of the Grubbs' catalyst (10-15 mol%) and titanium isopropoxide (0.3-3 equiv) provided ready access to α, β- unsaturated γ and δ-lactones and an important dipeptide isostere intermediate.

A Stereoselective Method for the Preparation of HIV-1 Protease Inhibitors Based on the Lewis Acid Mediated Reaction of Allylsilanes and N-Boc-α-amino Aldehydes

D'Aniello, Fabiana,Taddei, Maurizio

, p. 5247 - 5250 (2007/10/02)

-

L-687,908, a potent hydroxyethylene-containing HIV protease inhibitor [2]

Vacca,Guare,deSolms,Sanders,Giuliani,Young,Darke,Zugay,Sigal,Schleif,Quintero,Emini,Anderson,Huff

, p. 1225 - 1228 (2007/10/02)

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