CID 6450186

Base Information

• Chemical Name: CID 6450186
• CAS No.: 519-62-0
• Molecular Formula: C55H70MgN4O6
• Molecular Weight: 907.489
• Hs Code.: 29339900
• Wikipedia: Chlorophyll_b
• Mol file: 519-62-0.mol

Synonyms:chlorophyll b

Chemical Property of CID 6450186

Chemical Property:

• Appearance/Colour: green
• Vapor Pressure: 0mmHg at 25°C
• Melting Point: 183-185 °C(lit.)
• Boiling Point: 1071.6oC at 760mmHg
• Flash Point: 601.9oC
• PSA: 121.32000
• LogP: 9.13350
• Storage Temp.: 2-8°C
• Solubility.: Do you have solubility information on this product that you woul
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 22
• Exact Mass: 906.5145777
• Heavy Atom Count: 66
• Complexity: 2350

Purity/Quality:

98%,99%, ^*data from raw suppliers

Chlorophyllb(TechnicalGrade) ^*data from reagent suppliers

Safty Information:

• Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC1=C2C=C3C(=C4C(=O)C(C(=C4[N-]3)C5=NC(=CC6=NC(=CC(=N2)C1=C[O-])C(=C6C)C=C)C(C5CCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C)C)C(=O)OC)C.[Mg+2]
• Isomeric SMILES: CCC1=C2C=C3C(=C4C(=O)[C@@H](C(=C4[N-]3)C5=NC(=CC6=NC(=CC(=N2)C1=C[O-])C(=C6C)C=C)[C@H]([C@@H]5CCC(=O)OC/C=C(\C)/CCC[C@H](C)CCC[C@H](C)CCCC(C)C)C)C(=O)OC)C.[Mg+2]
• Uses: Do you have application information on this product that you would like to share Chlorophyll b is a photosynthetic pigment used in the absorption of light energy. Chlorophyl b is involved in photosynthesis and absorbs primarily blue light. Extends the absorption spectrum of light-harvesting complexes LHC-I and LHC-II above 700 nm

Technology Process of CID 6450186

There total 1 articles about CID 6450186 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

pheophytin b (3147-18-0,75498-61-2) → (10R)-Chlorophyll b (519-62-0) + (10S)-Chlorophyll b'

Guidance literature:

With lithium-di-t-butyl-4-methylphenoxide; In thiophene; at 50 ℃; for 0.5h; Yield given. Yields of byproduct given;

DOI:10.1002/hlca.19800630433

Reference yield: 100.0%

(10R)-Chlorophyll b (519-62-0) → pheophytin b (3147-18-0,75498-61-2)

Guidance literature:

With trichloroacetic acid; In tetrahydrofuran; Petroleum ether; for 0.25h;

Reference yield:

chlorophyll b (519-62-0) → pheophytin b (3147-18-0)

Guidance literature:

With hydrogenchloride; In diethyl ether; for 0.0166667h;

DOI:10.1021/ac00266a030

upstream raw materials:

pheophytin b

Downstream raw materials:

pheophytin b

pheophytin b

Refernces