Cas 1198077-22-3,(2R,4S)-4-(benzyloxy)hept-6-en-2-ol 2-(3,5-dimethoxyphenyl)acetate

1198077-22-3

Post Buying Request

Basic information

Product Name: (2R,4S)-4-(benzyloxy)hept-6-en-2-ol 2-(3,5-dimethoxyphenyl)acetate
Synonyms: (2R,4S)-4-(benzyloxy)hept-6-en-2-ol 2-(3,5-dimethoxyphenyl)acetate
CAS NO:1198077-22-3
Molecular Formula:
Molecular Weight: 398.499
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: (2R,4S)-4-(benzyloxy)hept-6-en-2-ol 2-(3,5-dimethoxyphenyl)acetate(CAS DataBase Reference)
NIST Chemistry Reference: (2R,4S)-4-(benzyloxy)hept-6-en-2-ol 2-(3,5-dimethoxyphenyl)acetate(1198077-22-3)
EPA Substance Registry System: (2R,4S)-4-(benzyloxy)hept-6-en-2-ol 2-(3,5-dimethoxyphenyl)acetate(1198077-22-3)

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: 1198077-22-3(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

1198077-22-3 Suppliers

Recommended suppliers

1198077-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1198077-22-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,0,7 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1198077-22:
(9*1)+(8*1)+(7*9)+(6*8)+(5*0)+(4*7)+(3*7)+(2*2)+(1*2)=183
183 % 10 = 3
So 1198077-22-3 is a valid CAS Registry Number.

1198077-22-3Upstream product

1198077-22-3Downstream Products

1198077-24-5 C₂₄H₃₂O₇

1198077-22-3Relevant academic research and scientific papers

Total synthesis of xestodecalactone c from L-malic acid

Yadav,Rao, Y. Gopala,Ravindar,Reddy, B. V. Subba,Narsaiah

experimental part, p. 3157 - 3161 (2009/12/27)

An efficient total synthesis of the ten-membered macrolide, xestodecalactone C is described. The synthetic sequence uses Barbier-allylation, LiAlH4/LiI-mediated syn-stereoselective 1,3-asymmetric reduction, and intramolecular Friedel-Crafts acylation as k

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 1198077-22-3