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(R)-2-METHYL-CBS-OXAZABOROLIDINE

(R)-2-METHYL-CBS-OXAZABOROLIDINE Structure
CAS No.
133261-83-3
Chemical Name:
(R)-2-METHYL-CBS-OXAZABOROLIDINE
Synonyms
(R)-ME CBS;(R)-METHYL OXAZABOROLIDINE;2-Methyl-CBS-oxazaborolidine;(R)-2-METHYL-CBS-OXAZABOROLIDINE MONOHYDRATE;(R)-3,3-diphenyl-1-methyltetrahydro-3H-pyrrolo-oxazaborole;(R)-5,5-DIPHENYL-2-METHYL-3,4-PROPANO-1,3,2-OXAZABOROLIDINE;ALPHA,ALPHA-DIPHENYL-D-PROLINOL METHYLBORONIC ACID CYCL-AMIDE-ESTER;(R)-1-METHYL,3,3-DIPHENYL-TETRAHYDRO-PYRROLO(1,2-C)(1,3,2)OXAZABOROLE;1-methyl-3,3-diphenyltetrahydro-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole;(R)-3,3-DIPHENYL-1-METHYLTETRAHYDRO-3H-PYRROLO-[1,2-C][1,3,2]OXAZABOROLE
CBNumber:
CB7431667
Molecular Formula:
C18H20BNO
Molecular Weight:
277.17
MOL File:
133261-83-3.mol

(R)-2-METHYL-CBS-OXAZABOROLIDINE Properties

Melting point 85-95 °C(lit.)
Boiling point 111 °C
Density 0.95 g/mL at 25 °C
Flash point 40 °F
storage temp. 2-8°C
pka 1.02±0.40(Predicted)

SAFETY

Risk and Safety Statements

Hazard Codes  F,Xn
Risk Statements  11-38-48/20-63-65-67
Safety Statements  36/37-62
RIDADR  UN 1294 3/PG 2
WGK Germany  3
10

(R)-2-METHYL-CBS-OXAZABOROLIDINE Preparation Products And Raw materials

Raw materials

Preparation Products

(R)-2-METHYL-CBS-OXAZABOROLIDINE Suppliers

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(R)-TETRAHYDRO-1-METHYL-3,3-DIPHENYL-1H,3H-PYRROLO[1,2-C][1,3,2] OXAZABOROLE (R)-TETRAHYDRO-1-METHYL-3,3-DIPHENYL-1H,3H-PYRROLO[1,2-C][1,3,2]OXAZOBOROLE (R)-METHYL OXAZABOROLIDINE (R)-ME CBS (R)-2-METHYL-CBS-OXAZABOROLIDINE MONOHYDRATE (R)-3,3-DIPHENYL-1-METHYLTETRAHYDRO-1H,3H-PYRROLO[1,2-C][1,3,2]OXAZABOROLE (R)-3,3-DIPHENYL-1-METHYLTETRAHYDRO-3H-PYRROLO-[1,2-C][1,3,2]OXAZABOROLE (R)-5,5-DIPHENYL-2-METHYL-3,4-PROPANO-1,3,2-OXAZABOROLIDINE ALPHA,ALPHA-DIPHENYL-D-PROLINOL METHYLBORONIC ACID CYCL-AMIDE-ESTER (R)-1-METHYL,3,3-DIPHENYL-TETRAHYDRO-PYRROLO(1,2-C)(1,3,2)OXAZABOROLE (R)-3,3-diphenyl-1-methyltetrahydro-3H-pyrrolo-oxazaborole 1H,3H-Pyrrolo[1,2-c][1,3,2]oxazaborole, tetrahydro-1-methyl-3,3-diphenyl- 2-Methyl-CBS-oxazaborolidine 1-methyl-3,3-diphenyltetrahydro-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole 133261-83-3 Reduction Asymmetric Synthesis B (Classes of Boron Compounds) B-Bromocatecholborane, etc. Chiral Catalysts, Ligands, and Reagents