35294-28-1
(R)-(+)-1,1-Bi-2-naphthol dimethyl ether
CAS: 35294-28-1
Molecular Formula: C22H18O2
35294-28-1 - Names and Identifiers
35294-28-1 - Physico-chemical Properties
| Molecular Formula | C22H18O2 |
| Molar Mass | 314.38 |
| Melting Point | 227-231°C(lit.) |
| BRN | 4704231 |
| Storage Condition | Inert atmosphere,Room Temperature |
| Use | Uses (R)-( )-2, 2-dimethoxy-1, 1 '-binaphthalene is a chiral compound and can be used as a chiral reagent. |
35294-28-1 - Risk and Safety
| Risk Codes | R41 - Risk of serious damage to eyes R50/53 - Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. R37/38 - Irritating to respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/39 - S60 - This material and its container must be disposed of as hazardous waste. S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. S36 - Wear suitable protective clothing. |
| UN IDs | UN 3077 9/PG 3 |
| WGK Germany | 3 |
35294-28-1 - Upstream Downstream Industry
| Downstream Products | (R)-3,3-DIBROMO-2,2-DIMETHOXY-1,1-BINAPHTHYL |
35294-28-1 - Nature
| optical activity (optical activity) | [α]20/D +52°, c = 1% in chloroform |
| BRN | 4704231 |
Last Update：2024-04-09 20:52:54
35294-28-1 - Uses and synthesis methods
introduction
Since the two enantiomers of (R)-( )-2, 2-dimethoxy -1, 1-binaphthalene are C2 symmetric bodies containing 2 identical binaphthalene rings, its rigid structure and C2 symmetry play an important role in chiral induction. It is an excellent chiral ligand and chiral auxiliary reagent, it is one of the most common structures in chiral synthesis, especially chiral catalysis.
Preparation
Using 1-bromo-2-methoxynaphthalene and 2-methoxynaphthalene-1-boric acid as starting materials, prepare the target compound (R)-( )-2, 2-dimethoxy-1, 1-binaphthalene
Last Update：2024-04-09 01:59:50
35294-28-1 - Reference Information
| introduction | due to (R)-( )-2,2 '-dimethoxy -1,1'-binaphthalene The two enantiomers are C2 symmetric bodies containing two identical binaphthalene rings, therefore, its rigid structure and C2 symmetry play an important role in chiral induction. It is an excellent chiral ligand and chiral auxiliary reagent, and is one of the most common structures in chiral synthesis, especially chiral catalysis. |
| use | (R)-( )-2,2 '-dimethoxy -1,1'-binaphthalene is a chiral compound and can be used as a chiral reagent. |
| preparation | the target compound (R)-( )-2,2 '-dimethoxy -1,1'-binaphthalene was prepared with 1-bromo -2-methoxy -1,1 '-boric acid as starting materials. the synthesis reaction formula is as follows: |
Last Update：2024-04-09 21:54:55
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Product Name: (R)-(+)-2,2-Dimethoxy-1,1-Binaphthyl Visit Supplier Webpage Request for quotation
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