Aladdin Scientific
(S)-DTBM-SEGPHOS (C007B-273830)
DescriptionTakasago Ligands and Complexes for Asymmetric ReactionsCatalytic ligand for:Enantioselective synthesis of secondary allylic alcohols via enantioselective reductions of α,β-unsaturated ketonesStereoselective preparation of cyclohexanone
DescriptionTakasago Ligands and Complexes for Asymmetric ReactionsCatalytic ligand for:Enantioselective synthesis of secondary allylic alcohols via enantioselective reductions of α,β-unsaturated ketonesStereoselective preparation of cyclohexanone derivatives via rhodium-catalyzed rearrangement of allyl or allenic cyclobutanolsCu-catalyzed asymmetric conjugate reduction of beta-substituted unsaturated phosphonates to give optically active beta-stereogenic alkylphosphonatesAsymmetric synthesis of cyclohexenones via Rh-catalyzed desymmetrization through enantioselective C-C bond activation and ring expansion of allenyl cyclobutanolsEnantioselective synthesis and crystal structure of P-stereogenic alkynylphosphine oxides by Rh-catalyzed [2+2+2] cycloaddition. Specification: 0.98 MDL Number: MFCD09753003 Molecular Formula: C74H100O8P2 Molecular Weight: 1179.53 PubChem CID: 11194192 Isomeric SMILES: CC(C)(C)C1=CC(=CC(=C1OC)C(C)(C)C)P(C2=C(C3=C(C=C2)OCO3)C4=C(C=CC5=C4OCO5)P(C6=CC(=C(C(=C6)C(C)(C)C)OC)C(C)(C)C)C7=CC(=C(C(=C7)C(C)(C)C)OC)C(C)(C)C)C8=CC(=C(C(=C8)C(C)(C)C)OC)C(C)(C)C Related Documents: https://ald-pub-files.oss-cn-shanghai.aliyuncs.com/aladdinsci/pdp/sds/1/S463308-SCI_655ec89f5af31628a4199b467c5e48d3.pdf
Specifications
- UPC:
- 51362400
- Condition:
- New
- Weight:
- 1.23 Ounces
- HazmatClass:
- No
- Quantity:
- 1
- Unit of Measurement:
- EA
- WeightUOM:
- LB
- MPN:
- S463308-5g
- CAS:
- 210169-40-7
- Product Size:
- 5g
- Hazard Statement Codes:
- H302:H315:H319:H335
- Precautionary Statement Codes:
- P261:P264:P271:P280:P302+P352:P304+P340:P305+P351+P338:P362+P364:P405:P403+P233:P501



