Cas 124817-98-7,(2S,3R,5S)-5-tert-Butoxycarbonylamino-3-carbamoyl-2,6-dimethyl-4-oxo-heptanoic acid benzyl ester

124817-98-7

Post Buying Request

Basic information

Product Name: (2S,3R,5S)-5-tert-Butoxycarbonylamino-3-carbamoyl-2,6-dimethyl-4-oxo-heptanoic acid benzyl ester
Synonyms:
CAS NO:124817-98-7
Molecular Formula:
Molecular Weight: 420.506
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: (2S,3R,5S)-5-tert-Butoxycarbonylamino-3-carbamoyl-2,6-dimethyl-4-oxo-heptanoic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3R,5S)-5-tert-Butoxycarbonylamino-3-carbamoyl-2,6-dimethyl-4-oxo-heptanoic acid benzyl ester(124817-98-7)
EPA Substance Registry System: (2S,3R,5S)-5-tert-Butoxycarbonylamino-3-carbamoyl-2,6-dimethyl-4-oxo-heptanoic acid benzyl ester(124817-98-7)

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: 124817-98-7(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

124817-98-7 Suppliers

Recommended suppliers

124817-98-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124817-98-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,8,1 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 124817-98:
(8*1)+(7*2)+(6*4)+(5*8)+(4*1)+(3*7)+(2*9)+(1*8)=137
137 % 10 = 7
So 124817-98-7 is a valid CAS Registry Number.

124817-98-7Upstream product

124817-98-7Downstream Products

108868-95-7 andrimid

124817-98-7Relevant academic research and scientific papers

Stereocontrolled Synthesis of Andrimid and a Structural Requirement for the Activity

McWhorter, William,Fredenhagen, Andreas,Nakanishi, Koji,Komura, Hajime

, p. 299 - 301 (1989)

Total synthesis of an antibiotic Andrimid was accomplished stereospecifically: it was shown that the chiralities at C-3 and C-4 should be R and S, respectively, and the presence of the (4S)-methyl group is important for the activity.

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 124817-98-7