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Tert-butyl+6-methylbenzo[d][1,3]dioxole-5-carboxylate
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Tert-butyl+6-methylbenzo[d][1,3]dioxole-5-carboxylate
Catalog Number:
(10434-818)
Supplier:
Bioss
Description:
TEM7R also known as PLXDC2 is a 529 amino acid single-pass type I membrane protein containing one PSI domain and belonging to the plexin family. Localizing to membrane, TEM7R is expressed in endothelial cells of the stroma, as well as in limbs, lung buds, developing heart, spinal cord and dorsal root ganglia. TEM7R interacts with cortactin and may play a role in tumor angiogenesis. Existing as three alternatively spliced isoforms, the gene encoding TEM7R maps to human chromosome 10p12.31. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Catalog Number:
(TCP0876-025ML)
Supplier:
TCI America
Description:
CAS Number: 2344-70-9
MDL Number: MFCD00044349 Molecular Formula: C10H14O Molecular Weight: 150.22 Purity/Analysis Method: >99.0% (GC) Form: Clear Liquid Color: Colorless Boiling point (°C): 239 Flash Point (°C): 110 Specific Gravity (20/20): 0.98
Catalog Number:
(10283-060)
Supplier:
Bioss
Description:
PTCHD3 is a 767 amino acid multi-pass membrane protein that localizes to the midpiece of the sperm tail, where it is implicated in sperm function and development. A member of the patched family, PTCHD3 contains one SSD (sterol-sensing) domain and is encoded by a gene that maps to human chromosome 10p12.1. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Catalog Number:
(10283-062)
Supplier:
Bioss
Description:
PTCHD3 is a 767 amino acid multi-pass membrane protein that localizes to the midpiece of the sperm tail, where it is implicated in sperm function and development. A member of the patched family, PTCHD3 contains one SSD (sterol-sensing) domain and is encoded by a gene that maps to human chromosome 10p12.1. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Catalog Number:
(10278-346)
Supplier:
Bioss
Description:
PTCHD3 is a 767 amino acid multi-pass membrane protein that localizes to the midpiece of the sperm tail, where it is implicated in sperm function and development. A member of the patched family, PTCHD3 contains one SSD (sterol-sensing) domain and is encoded by a gene that maps to human chromosome 10p12.1. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Supplier:
BeanTown Chemical
Description:
CAS: 589-15-1; EC No: 209-636-5; MDL No: MFCD00000179
UN No: UN1759; Haz Class: 8; Packing Group: II
Crystalline; Molecular Formula: C7H6Br2; MW: 249.93
Melting Point: 62-64°
Supplier:
Thermo Scientific Chemicals
Description:
Fieser: 1,508 15,258 16,275 17,280 18,290 19,268 20,305 21,343
Supplier:
Thermo Scientific Chemicals
Description:
Methylbenzene. Grade:99, Melting Point ca -93*. Boiling Point C:110-111*. C7H8. 108-88-3. HIGHLY FLAMMABLE HARMFUL
Supplier:
AMBEED, INC
Description:
4-tert-Butyl-o-xylene 99+%
Supplier:
AMBEED, INC
Description:
4-Allylveratrole ≥95%
Catalog Number:
(77417-956)
Supplier:
APOLLO SCIENTIFIC
Description:
4-(Trifluoromethoxy)phenyl isocyanate 98%
Supplier:
AMBEED, INC
Description:
4-Propenylveratrole 98%
Supplier:
AMBEED, INC
Description:
3,5-Di-tert-butylpyrocatechol 95%
Supplier:
TCI America
Description:
CAS Number: 124061-43-4
MDL Number: MFCD04039747 Molecular Formula: C16H16N2O4 Molecular Weight: 300.31 Purity/Analysis Method: >98.0% (HPLC,N) Form: Powder Melting point (°C): 250
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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