156715-37-6

• 

• Basic information

  1. Product Name: (+)-[1(S)-(1alpha,2alpha,3alpha,4alpha)]-3-[2-[3-[4-(N-Pentylcarbamoyl)oxazol-2-yl]-7-oxabicyclo[2.2.1]hept-2-ylmethyl]phenyl]propanoic acid monosodium salt
  2. Synonyms: Ifetroban sodium; BMS-180291-02; BMS-180291 sodium salt; (+)-[1S-(exo,exo)]-2-[[3-[4-[(n-Pentylamino)carbonyl]-2-oxazolyl]-7-oxabicyclo[2.2.1]hept-2-yl]methyl]benzenepropanoic acid monosodium salt
  3. CAS NO:156715-37-6
  4. Molecular Formula: C₂₅H₃₁N₂NaO₅
  5. Molecular Weight: 462.52602
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 156715-37-6.mol
  9. Article Data: 3

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: N/A
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: (+)-[1(S)-(1alpha,2alpha,3alpha,4alpha)]-3-[2-[3-[4-(N-Pentylcarbamoyl)oxazol-2-yl]-7-oxabicyclo[2.2.1]hept-2-ylmethyl]phenyl]propanoic acid monosodium salt(CAS DataBase Reference)
  10. NIST Chemistry Reference: (+)-[1(S)-(1alpha,2alpha,3alpha,4alpha)]-3-[2-[3-[4-(N-Pentylcarbamoyl)oxazol-2-yl]-7-oxabicyclo[2.2.1]hept-2-ylmethyl]phenyl]propanoic acid monosodium salt(156715-37-6)
  11. EPA Substance Registry System: (+)-[1(S)-(1alpha,2alpha,3alpha,4alpha)]-3-[2-[3-[4-(N-Pentylcarbamoyl)oxazol-2-yl]-7-oxabicyclo[2.2.1]hept-2-ylmethyl]phenyl]propanoic acid monosodium salt(156715-37-6)

• 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: 156715-37-6(Hazardous Substances Data)

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156715-37-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156715-37-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,7,1 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 156715-37:
(8*1)+(7*5)+(6*6)+(5*7)+(4*1)+(3*5)+(2*3)+(1*7)=146
146 % 10 = 6
So 156715-37-6 is a valid CAS Registry Number.

156715-37-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name	ifetroban sodium

1.2 Other means of identification

Product number	-
Other names	[1S-(1α,2α,3α,4α)]-2-[[3-[4-[(Pentylamino)carbonyl]-2-oxazolyl]-7-oxabicyclo[2.2.1]hept-2-yl]methyl]benzenepropanoic acid,monosodium salt

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:156715-37-6 SDS

156715-37-6Upstream product

156715-37-6Downstream Products

156715-37-6Relevant articles and documents

Method for preparing homochiral maleimide intermediates, via silylation techniques

-

, (2008/06/13)

A method is provided for preparing homochiral maleimide intermediates of the structure STR1 wherein R7, R8 and R9 are as defined herein by reacting a homochiral amine of the structure STR2 with maleic anhydride and a silylating agent. The maleimide intermediate is used in the enantio-selective preparation of thromboxane A2 receptor antagonists.

Method for preparing a benzaldehyde intermediate

-

, (2008/06/13)

A method is provided for preparing a chiral benzaldehyde of the structure STR1 by acylating an anhydride of the structure STR2 with a chiral oxazolidine of the structure STR3 where Q is MgHal or Li, and X, Y and Z are as described herein, to form a keto acid which is reduced and cyclized. The resulting benzaldehyde may be used in making the final anti-thrombotic - anti-vasospastic compounds. Novel intermediates are also provided.

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