Cas 1233194-97-2,(S)-N-tert-butoxycarbonyl-(3-benzyloxy-2-chloro-4-methoxy)phenylalanine methyl ester

1233194-97-2

Post Buying Request

Basic information

Product Name: (S)-N-tert-butoxycarbonyl-(3-benzyloxy-2-chloro-4-methoxy)phenylalanine methyl ester
Synonyms:
CAS NO:1233194-97-2
Molecular Formula:
Molecular Weight: 449.931
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: (S)-N-tert-butoxycarbonyl-(3-benzyloxy-2-chloro-4-methoxy)phenylalanine methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-N-tert-butoxycarbonyl-(3-benzyloxy-2-chloro-4-methoxy)phenylalanine methyl ester(1233194-97-2)
EPA Substance Registry System: (S)-N-tert-butoxycarbonyl-(3-benzyloxy-2-chloro-4-methoxy)phenylalanine methyl ester(1233194-97-2)

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: 1233194-97-2(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

1233194-97-2 Suppliers

Recommended suppliers

1233194-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1233194-97-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,3,1,9 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1233194-97:
(9*1)+(8*2)+(7*3)+(6*3)+(5*1)+(4*9)+(3*4)+(2*9)+(1*7)=142
142 % 10 = 2
So 1233194-97-2 is a valid CAS Registry Number.

1233194-97-2Upstream product

100-39-0 benzyl bromide

1233194-97-2Downstream Products

220903-34-4 (S)-N-tert-butyloxycarbonyl-(3-benzyloxy-2-chloro-4-methoxy)-phenylalanine

1233194-97-2Relevant academic research and scientific papers

Highly stereoselective and efficient synthesis of the dopa analogue in pepticinnamin E via enantioselective hydrogenation of dehydroamino acids

Sun, Dequn

, p. 181 - 186 (2010)

An efficient and new method was developed to prepare the dopa analogue 11 in natural pepticinnamin via catalytic hydrogenation of dehydroamino acids (DDAA) with a good yield and ee. Product 11 is a key intermediate towards the total synthesis of pepticinnamin E and its analogues. TUeBITAK.

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 1233194-97-2