150840-32-7

• 

• Basic information

  1. Product Name: 11-{[(3alpha)-3-hydroxy-28-oxolup-20(29)-en-28-yl]amino}undecanoic acid
  2. Synonyms: Undecanoic acid, 11-[[(3α)-3-hydroxy-28-oxolup-20(29)-en-28-yl]amino]- (9CI)
  3. CAS NO:150840-32-7
  4. Molecular Formula: C₄₁H₆₉NO₄
  5. Molecular Weight: 639.9909
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 150840-32-7.mol
  9. Article Data: 6

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 738.9°C at 760 mmHg
  3. Flash Point: 400.7°C
  4. Appearance: N/A
  5. Density: 1.038g/cm³
  6. Vapor Pressure: 3.34E-25mmHg at 25°C
  7. Refractive Index: 1.521
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. PKA: 4.78±0.10(Predicted)
  11. CAS DataBase Reference: 11-{[(3alpha)-3-hydroxy-28-oxolup-20(29)-en-28-yl]amino}undecanoic acid(CAS DataBase Reference)
  12. NIST Chemistry Reference: 11-{[(3alpha)-3-hydroxy-28-oxolup-20(29)-en-28-yl]amino}undecanoic acid(150840-32-7)
  13. EPA Substance Registry System: 11-{[(3alpha)-3-hydroxy-28-oxolup-20(29)-en-28-yl]amino}undecanoic acid(150840-32-7)

• 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: 150840-32-7(Hazardous Substances Data)

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• Undecanoic acid,11-[[(3a)-3-hydroxy-28-oxolup-20(29)-en-28-yl]amino]-(9CI)

  Cas No: 150840-32-7

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• 10 Gram

• 500 Kilogram/Month

• Zibo Hangyu Biotechnology Development Co., Ltd
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• Undecanoic acid,11-[[(3a)-3-hydroxy-28-oxolup-20(29)-en-28-yl]amino]-(9CI)

  Cas No: 150840-32-7

• No Data

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150840-32-7 Usage

Chemical structure

A chemical compound containing a fatty acid chain with an amino group attached to a lupane structure.

Fatty acid chain

The compound has an undecanoic acid chain, which is an 11-carbon long fatty acid.

Amino group attachment

The amino group is attached to the lupane structure, forming an amino linkage.

Lupane structure

The lupane structure is characterized by a 28-oxo and a 3-hydroxy group.

Stereochemistry

The compound has a 3alpha configuration, indicating the position of the hydroxyl group on the lupane structure.

Biological activities

The compound may have potential biological activities, such as anti-inflammatory, anticancer, or antimicrobial properties.

Further research

More research is needed to fully understand the potential uses and effects of this chemical.

Molecular weight

The molecular weight of the compound is approximately 658.02 g/mol.

Solubility

The compound's solubility properties are not explicitly mentioned, but it is likely to be soluble in organic solvents due to its fatty acid chain.

Stability

The stability of the compound is not explicitly mentioned, but it may be sensitive to heat, light, and oxidation due to the presence of a hydroxyl group and a double bond in the lupane structure.

Synthesis

The synthesis of the compound may involve the formation of an amide bond between the amino group of the lupane structure and the carboxylic acid group of the undecanoic acid.

Applications

The potential applications of the compound are not explicitly mentioned, but it may be used in the development of new drugs or as a research tool for studying biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 150840-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,8,4 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 150840-32:
(8*1)+(7*5)+(6*0)+(5*8)+(4*4)+(3*0)+(2*3)+(1*2)=107
107 % 10 = 7
So 150840-32-7 is a valid CAS Registry Number.

150840-32-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	11-[[(1R,3aS,5aR,5bR,7aR,9R,11aR,11bR,13aR,13bR)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carbonyl]amino]undecanoic acid

1.2 Other means of identification

Product number	-
Other names	-

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:150840-32-7 SDS

150840-32-7Upstream product

• 28691-27-2 methyl 11-aminoundecanoate 
• 150840-96-3 11-[((1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-Acetoxy-1-isopropenyl-5a,5b,8,8,11a-pentamethyl-icosahydro-cyclopenta[a]chrysene-3a-carbonyl)-amino]-undecanoic acid methyl ester 
• 60-29-7 diethyl ether 
• 10376-50-8 3-O-acetylbetulinic acid 
• 59868-82-5 3-O-acetylbetulinic acid chloride 

150840-32-7Downstream Products

150840-32-7Relevant articles and documents

Synthesis and anti-HIV activity of bi-functional betulinic acid derivatives

Huang, Li,Ho, Phong,Lee, Kuo-Hsiung,Chen, Chin-Ho

, p. 2279 - 2289 (2007/10/03)

Betulinic acid (BA) derivatives with a side chain at C-3 can inhibit HIV-1 maturation. On the other hand, BA derivatives with a side chain at C-28 can block HIV-1 entry. In order to combine the anti-maturation and anti-entry activities in a single molecul

Anti-AIDS agents 49. Synthesis, anti-HIV, and anti-fusion activities of IC9564 analogues based on betulinic acid

Sun, I-Chen,Chen, Chin-Ho,Kashiwada, Yoshiki,Wu, Jiu-Hong,Wang, Hui-Kang,Lee, Kuo-Hsiung

, p. 4271 - 4275 (2007/10/03)

The betulinic acid derivative IC9564 inhibits human immunodeficiency virus (HIV)-1 entry. Among a series of IC9564 derivatives, 5 and 20 were the most promising compounds against HIV infection with EC50 values of 0.33 and 0.46 μM, respectively.

Betulinic acid derivatives: A new class of specific inhibitors of human immunodeficiency virus type 1 entry

Soler, Fran?oise,Poujade, Christèle,Evers, Michel,Carry, Jean-Christophe,Hénin, Yvette,Bousseau, Anne,Huet, Thierry,Pauwels, Rudi,De Clercq, Erik,Mayaux, Jean-Fran?ois,Le Pecq, Jean-Bernard,Dereu, Norbert

, p. 1069 - 1083 (2007/10/03)

A novel series of ω-aminoalkanoic acid derivatives of betulinic acid were synthesized and evaluated for their activity against human immunodeficiency virus (HIV). The anti-HIV-1 activity of several members of this new series was found to be in the nanomolar range in CEM 4 and MT-4 cell cultures. The optimization of the ω-aminoalkanoic acid side chain is described. The presence of an amide function within the side chain was found important for optimal activity. RPR 103611 (14g), a statine derivative, was found to be inactive against HIV-1 protease, reverse transcriptase, and integrase as well as on gp120/CD4 binding. 'Time of addition' experiments suggested interaction with an early step of HIV-1 replication. As syncytium formation, but not virus-cell binding, seems to be affected, betulinic acid derivatives are assumed to interact with the postbinding virus-cell fusion process.

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