Cas 133706-85-1,(E)-(S)-5-[3-(4-Fluoro-phenyl)-5-isopropyl-2-phenyl-3H-imidazol-4-yl]-3-hydroxy-pent-4-enoic acid methyl ester

133706-85-1

Post Buying Request

Basic information

Product Name: (E)-(S)-5-[3-(4-Fluoro-phenyl)-5-isopropyl-2-phenyl-3H-imidazol-4-yl]-3-hydroxy-pent-4-enoic acid methyl ester
Synonyms:
CAS NO:133706-85-1
Molecular Formula:
Molecular Weight: 408.473
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (E)-(S)-5-[3-(4-Fluoro-phenyl)-5-isopropyl-2-phenyl-3H-imidazol-4-yl]-3-hydroxy-pent-4-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-(S)-5-[3-(4-Fluoro-phenyl)-5-isopropyl-2-phenyl-3H-imidazol-4-yl]-3-hydroxy-pent-4-enoic acid methyl ester(133706-85-1)
EPA Substance Registry System: (E)-(S)-5-[3-(4-Fluoro-phenyl)-5-isopropyl-2-phenyl-3H-imidazol-4-yl]-3-hydroxy-pent-4-enoic acid methyl ester(133706-85-1)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 133706-85-1(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

133706-85-1 Suppliers

Recommended suppliers

133706-85-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133706-85-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,7,0 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 133706-85:
(8*1)+(7*3)+(6*3)+(5*7)+(4*0)+(3*6)+(2*8)+(1*5)=121
121 % 10 = 1
So 133706-85-1 is a valid CAS Registry Number.

133706-85-1Upstream product

133706-85-1Downstream Products

133706-85-1Relevant academic research and scientific papers

Stereoselective Aldol Reaction with Chiral Acetates

Prasad, Kapa,Chen, Kau-Ming,Repic, Oljan,Hardtmann, Goetz E.

, p. 703 - 706 (2007/10/02)

The synthesis of enantiomerically pure 5 is described utilizing chiral acetate 2 and aldehyde 3 employing novel aldol reaction conditions (e.g., the use of excess organic amine compared to n-BuLi for generating the enolate).In addition, some interesting new chiral auxiliaries are also described.

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

What can I do for you?
Get Best Price

Get Best Price for 133706-85-1