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L-Alanine, N-(cyclohexylcarbonyl)-, 11-ester with 20,23-didehydro-20,2 3-dideoxo-20,23-dihydroxyansatrienol A is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • L-Alanine, N-(cyclohexylcarbonyl)-, 11-ester with 20,23-didehydro-20,2 3-dideoxo-20,23-dihydroxyansatrienol A

    Cas No: 80111-48-4

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  • Wuhan Wonda Pharm Limited
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  • 80111-48-4 Structure
  • Basic information

    1. Product Name: L-Alanine, N-(cyclohexylcarbonyl)-, 11-ester with 20,23-didehydro-20,2 3-dideoxo-20,23-dihydroxyansatrienol A
    2. Synonyms: L-Alanine, N-(cyclohexylcarbonyl)-, 11-ester with 20,23-didehydro-20,2 3-dideoxo-20,23-dihydroxyansatrienol A
    3. CAS NO:80111-48-4
    4. Molecular Formula: C36H50N2O8
    5. Molecular Weight: 638.797
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 80111-48-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 834.5°C at 760 mmHg
    3. Flash Point: 458.5°C
    4. Appearance: /
    5. Density: 1.21g/cm3
    6. Vapor Pressure: 1.54E-29mmHg at 25°C
    7. Refractive Index: 1.588
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: L-Alanine, N-(cyclohexylcarbonyl)-, 11-ester with 20,23-didehydro-20,2 3-dideoxo-20,23-dihydroxyansatrienol A(CAS DataBase Reference)
    11. NIST Chemistry Reference: L-Alanine, N-(cyclohexylcarbonyl)-, 11-ester with 20,23-didehydro-20,2 3-dideoxo-20,23-dihydroxyansatrienol A(80111-48-4)
    12. EPA Substance Registry System: L-Alanine, N-(cyclohexylcarbonyl)-, 11-ester with 20,23-didehydro-20,2 3-dideoxo-20,23-dihydroxyansatrienol A(80111-48-4)
  • 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: 80111-48-4(Hazardous Substances Data)

80111-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80111-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,1,1 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80111-48:
(7*8)+(6*0)+(5*1)+(4*1)+(3*1)+(2*4)+(1*8)=84
84 % 10 = 4
So 80111-48-4 is a valid CAS Registry Number.
InChI:InChI=1/C36H50N2O8/c1-23-14-13-17-27-20-28(39)21-30(34(27)42)38-32(40)22-29(45-4)18-11-6-5-7-12-19-31(24(2)33(23)41)46-36(44)25(3)37-35(43)26-15-9-8-10-16-26/h5-7,11-12,14,18,20-21,24-26,29,31,33,39,41-42H,8-10,13,15-17,19,22H2,1-4H3,(H,37,43)(H,38,40)/b6-5+,12-7+,18-11-,23-14-/t24-,25+,29-,31-,33-/m0/s1

80111-48-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [(4Z,6R,7R,8S,10Z,12Z,14Z,16R)-6,22,24-trihydroxy-16-methoxy-5,7-dimethyl-18-oxo-19-azabicyclo[18.3.1]tetracosa-1(23),4,10,12,14,20(24),21-heptaen-8-yl] (2R)-2-(cyclohexanecarbonylamino)propanoate

1.2 Other means of identification

Product number -
Other names Ansatrienin B

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:80111-48-4 SDS

80111-48-4Downstream Products

80111-48-4Relevant articles and documents

Ansamycin antibiotics as free radical scavengers isolated from Streptomyces by using the bactericidal action of the hydroxyl radical

Morimitsu, Yasujiro,Hirota, Akira

, p. 1507 - 1509 (1996)

Ansamycin antibiotics (1-4) were isolated from the cultured broth of Streptomyces sp. USF-319 strain as a result of our screening for free radical scavengers. They inhibited the bactericidal effect of the Fenton reagent toward Bacillus subtilis by their radical scavenging activity. Some of them also showed inhibitory activity against lipid peroxidation and lipoxygenases.

New ansamycin derivatives generated by simultaneous mutasynthesis

Song, Ya Nan,Jiao, Rui Hua,Zhang, Wen Jing,Zhao, Guo Yan,Dou, Huan,Jiang, Rong,Zhang, Ai Hua,Hou, Ya Yi,Bi, Shu Feng,Ge, Hui Ming,Tan, Ren Xiang

, p. 556 - 559 (2015)

The conversion from triene- to diene-typed ansamycins is clarified step by step in Streptomyces seoulensis IFB-A01. Such an intertype convertibility is adopted to establish for the first time the simultaneous mutasynthesis of both types of C17-benzene ans

(+)-Mycotrienins I and II: Relative and absolute stereochemistry

Smith III,Wood,Omura

, p. 841 - 842 (1991)

The complete relative and absolute stereochemistry of the potent antifungal antibiotics (+)-mycotrienin I and (+)-mycotrienin II have been established by chemical correlation with the antitumor agent (+)-trienomycin A.

(+)-Trienomycins A, B, C, and F and (+)-mycotrienins I and II: Relative and absolute stereochemistry

Smith III, Amos B.,Wood, John L.,Wong, Weichyun,Gould, Alexandra E.,Rizzo, Carmelo J.,Barbosa, Joseph,Komiyama, Kanki,Omura, Satoshi

, p. 8308 - 8315 (2007/10/03)

The complete relative and absolute stereochemistries have been elucidated for the ansamycin antibiotics (+)-trienomycins A, B, and C and their potent antifungal congeners, the (+)-mycotrienins I and II. A new species, (+)-trienomycin F, has also been isol

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