306371
2-(Chloromethyl)tetrahydro-2H-pyran
99%
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About This Item
Empirical Formula (Hill Notation):
C6H11ClO
CAS Number:
Molecular Weight:
134.60
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
2-(Chloromethyl)tetrahydro-2H-pyran, 99%
InChI
1S/C6H11ClO/c7-5-6-3-1-2-4-8-6/h6H,1-5H2
SMILES string
ClCC1CCCCO1
InChI key
PPYKTTGONDVGPX-UHFFFAOYSA-N
assay
99%
refractive index
n20/D 1.462 (lit.)
bp
53-54 °C/12 mmHg (lit.)
density
1.075 g/mL at 25 °C (lit.)
functional group
chloro
ether
Application
2-(Chloromethyl)tetrahydro-2H-pyran may be used in chemical synthesis studies.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
131.0 °F - closed cup
flash_point_c
55 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Jun Zhao et al.
Cell metabolism, 31(5), 937-955 (2020-04-24)
Cell proliferation and inflammation are two metabolically demanding biological processes. How these competing processes are selectively executed in the same cell remains unknown. Here, we report that the enzyme carbamoyl-phosphate synthetase, aspartyl transcarbamoylase, and dihydroorotase (CAD) deamidates the RelA subunit
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