UR7Pnm6zmh

Base Information

• Chemical Name: UR7Pnm6zmh
• CAS No.: 67671-05-0
• Molecular Formula: C₈H₁₂O
• Molecular Weight: 124.183
• UNII: UR7PNM6ZMH
• Nikkaji Number: J231.994B

Synonyms:UR7PNM6ZMH;UNII-UR7PNM6ZMH;J231.994B;(1beta,4beta)-Norborna-5-ene-2beta-methanol;Bicyclo(2.2.1)hept-5-ene-2-methanol, (1R-exo)-;(1R,2S,4R)-Bicyclo(2.2.1)hept-5-ene-2-methanol;Bicyclo(2.2.1)hept-5-ene-2-methanol, (1R,2S,4R)-;67671-05-0;(1beta,2beta,4beta)-Bicyclo(2.2.1)hept-5-ene-2-methanol;SCHEMBL2282146;(1.BETA.,4.BETA.)-NORBORNA-5-ENE-2.BETA.-METHANOL;(1.BETA.,2.BETA.,4.BETA.)-BICYCLO(2.2.1)HEPT-5-ENE-2-METHANOL

Chemical Property of UR7Pnm6zmh

Chemical Property:

• XLogP3: 1.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 124.088815002
• Heavy Atom Count: 9
• Complexity: 140

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1C2CC(C1C=C2)CO
• Isomeric SMILES: C1[C@@H]2C[C@@H]([C@H]1C=C2)CO

Technology Process of UR7Pnm6zmh

There total 88 articles about UR7Pnm6zmh 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: 100.0%

(+)-(1R,4R,5S)-bicyclo<2.2.1>hept-2-ene-5-carboxylic acid (120-74-1,934-30-5,1195-12-6,20507-53-3,58001-99-3,67999-50-2,74645-32-2,108266-75-7,67999-53-5) → exo-bicyclo<2.2.1>hept-5-en-2-methanol (67671-05-0)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 2h; Inert atmosphere; Reflux;

DOI:10.1039/c5cc07882b

Reference yield: 100.0%

methyl exo-5-norbornene-2-carboxylate (769-85-7) → 5-norbornene-2-methanol (13360-81-1,15507-06-9,42070-72-4,42070-82-6,67505-46-8,67671-05-0,67671-06-1,69831-10-3,95-12-5)

Guidance literature:

With lithium aluminium tetrahydride; In diethyl ether; for 8h; Heating;

DOI:10.1002/hlca.19800630422

Reference yield: 99.0%

exo-2-formylbicyclo[2.2.1]hept-5-ene (5453-80-5,19926-88-6,19926-90-0,58001-94-8,69831-12-5,69831-13-6,72203-35-1,96443-40-2,96443-41-3) → 5-norbornene-2-methanol (13360-81-1,15507-06-9,42070-72-4,42070-82-6,67505-46-8,67671-05-0,67671-06-1,69831-10-3,95-12-5)

Guidance literature:

With sodium tetrahydroborate; In methanol; water; at 20 ℃; for 1h;

DOI:10.1016/S0040-4020(02)01053-0

upstream raw materials:

(1S,2S,4S)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid

endo-norbornenecarboxylic acid

ethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate

(-)-menthyl acrylate

Downstream raw materials:

Toluene-4-sulfonic acid (1S,2S,4S)-1-bicyclo[2.2.1]hept-5-en-2-ylmethyl ester

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