Benzyl bromoacetate - CAS 5437-45-6
Catalog: |
BB028626 |
Product Name: |
Benzyl bromoacetate |
CAS: |
5437-45-6 |
Synonyms: |
benzyl 2-bromoacetate |
IUPAC Name: | benzyl 2-bromoacetate |
Description: | Benzyl bromoacetate (CAS# 5437-45-6) is used in the synthesis of somatostatin analogues with tumor-targeting properties . Also used in the synthesis of inhibitors of phospholipase A2, indolizine and indene derivatives. |
Molecular Weight: | 229.07 |
Molecular Formula: | C9H9BrO2 |
Canonical SMILES: | C1=CC=C(C=C1)COC(=O)CBr |
InChI: | InChI=1S/C9H9BrO2/c10-6-9(11)12-7-8-4-2-1-3-5-8/h1-5H,6-7H2 |
InChI Key: | JHVLLYQQQYIWKX-UHFFFAOYSA-N |
Boiling Point: | 166-170 °C (22 mmHg) |
Density: | 1.446 g/cm3 |
Appearance: | Colorless or light yellow liquid |
Storage: | Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances. |
MDL: | MFCD00000190 |
LogP: | 2.12470 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
WO-2021207172-A1 | Compounds and methods for targeted degradation of kras | 20200406 |
WO-2021203025-A1 | 1 h-pyrazolo[4,3-g]isoquinoline and 1 h-pyrazolo[4,3-g]quinoline derivatives as alpha-1 -antitrypsin modulators for treating alpha-1 -antitrypsin deficiency (aatd) | 20200403 |
WO-2021190727-A1 | Compounds and their use in the treatment of bacterial infection | 20200324 |
WO-2021188537-A1 | Selective small molecule degraders of cereblon | 20200317 |
JP-2021147400-A | Ink, inkjet printing method and printing media | 20200316 |
PMID | Publication Date | Title | Journal |
22409381 | 20120401 | Light-harvesting cross-linked polymers for efficient heterogeneous photocatalysis | ACS applied materials & interfaces |
22848796 | 20120101 | Convenient and scalable synthesis of fmoc-protected Peptide nucleic Acid backbone | Journal of nucleic acids |
21542562 | 20110728 | Novel lipophilic acetohydroxamic acid derivatives based on conformationally constrained spiro carbocyclic 2,6-diketopiperazine scaffolds with potent trypanocidal activity | Journal of medicinal chemistry |
19118822 | 20090217 | Regioselective synthesis of a glycomimetic trisaccharide of Sialyl Lewis (sLex) | Carbohydrate research |
853505 | 19770501 | Synthesis and anti-herpes simplex activity of analogues of phosphonoacetic acid | Journal of medicinal chemistry |
Complexity: | 142 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 227.97859 |
Formal Charge: | 0 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 227.97859 |
Rotatable Bond Count: | 4 |
Topological Polar Surface Area: | 26.3 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.8 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Carbonyl Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS