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Methyl+2-amino-3,5-difluorobenzoate
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Methyl+2-amino-3,5-difluorobenzoate
Catalog Number:
(89151-336)
Supplier:
Enzo Life Sciences
Catalog Number:
(AAH28265-03)
Supplier:
Thermo Scientific Chemicals
Description:
1g CAS: 80938-67-6, MDL: MFCD00270126
Catalog Number:
(77697-174)
Supplier:
LGC STANDARDS
Description:
Methyl [[4-[2-[(5-Chloro-2-methoxybenzoyl)amino]ethyl]phenyl]sulphonyl]carbamate, Mikromol, LGC Standards
Supplier:
ALADDIN SCIENTIFIC
Description:
Voltammetric behavior of 2-amino-6-nitrobenzothiazole has been investigated using direct current voltammetry and differential pulse voltammetry2-Amino-6-nitrobenzothiazole has been used: . as model analyte for voltammetric determination of electrochemically reducible organic substances[4] . in the synthesis of 2-methyl-4-nitro-2H-pyrazole-3-carboxylic acid[2-(cyclohexanecarbonylamino)benzothiazol-6-yl]amide derivatives . in the preparation of push-pull nonlinear optical chromophores containing thiazole and benzothiazole acceptors . as a base in dye production by diazotation reaction
Supplier:
TCI America
Description:
CAS Number: 951-55-3
MDL Number: MFCD00005652 Molecular Formula: C12H14N2O2 Molecular Weight: 218.26 Purity/Analysis Method: >98.0% (T,HPLC) Form: Crystal Melting point (°C): 275 Specific rotation [a]20/D: 0 deg (C=1, HCl)
Catalog Number:
(10448-594)
Supplier:
Bioss
Description:
CGI-99 is a 244 amino acid protein that localizes to the nucleus, as well as to the cytoplasm, and belongs to the UPF0568 family. Expressed in a variety of tissues with particularly high levels in heart and skeletal muscle, CGI-99 functions as a homodimer that interacts with Ninein and is thought to regulate Ninein function. CGI-99 is overexpressed in brain tumor tissue, suggesting a role in tumor development and metastasis. The gene encoding CGI-99 maps to human chromosome 14, which houses over 700 genes and comprises nearly 3.5% of the human genome. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease (AD). The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder ?-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction.
Supplier:
AMBEED, INC
Description:
4-(1-Hydroxyethyl)aniline, Purity: 98%, CAS Number: 14572-89-5, Appearance: Form: solid Colour: Pale-yellow to Yellow, Storage: Keep in dark place, Inert atmosphere, 2-8 C, Size: 1g
Catalog Number:
(102537-216)
Supplier:
Matrix Scientific
Description:
MF=C9H11NO2 MW=165.19 CAS=35613-44-6 MDL=MFCD04973395 1G
Supplier:
AMBEED, INC
Description:
Sorafenib tosylate (BAY 43-9006 tosylate salt) 98%
Supplier:
RPI
Description:
Bisacrylamide
Catalog Number:
(10072-786)
Supplier:
Prosci
Description:
DKK-1 is a member of the DKK protein family which also includes DKK-2, DKK-3 and DKK-4. DKK-1 was originally identified as a Xenopus head forming molecule that behaves as an antagonist for Wnt signaling. Subsequent studies have shown that DKK-1 and DKK-4 play an important regulatory role in the Wnt /β-catenin signaling pathway by forming inhibitory complexes with LDL receptor-related proteins 5 and 6 (LRP5 and LRP6), which are essential components of the Wnt/βcatenin signaling system. LPR5 and LPR6 are single-pass transmembrane proteins that appear to act as co-receptors for Wnt ligands involved in the Wnt/βcatenin signaling cascade. It has been suggested that by inhibiting Wnt/β-catenin signaling, which is essential for posterior patterning in vertebrates, DKK-1 permits anterior development. This notion is supported by the finding that mice deficient of DKK-1 expression lack head formation and die during embryogenesis. Recombinant human DKK-1 expressed in human 293 cells is a 35-40 kDa glycoprotein containing 235 amino-acid residues.
Supplier:
Spectrum Chemicals
Description:
Guanosine 5'-Triphosphate, Sodium Salt is a purine nucleoside triphosphate which plays a role as an activator of substrates in metabolic reactions.
Supplier:
AMBEED, INC
Description:
Fmoc-Lys-OMe.HCl, Purity: 97%, CAS number: 847658-45-1, Appearance: Solid, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 250MG
Catalog Number:
(103665-034)
Supplier:
Sino Biological
Description:
A DNA sequence encoding the mouse CADM3 (NP_444429.1) extracellular domain (Met 1-His 328) was expressed, with a polyhistidine tag at the C-terminus.
Catalog Number:
(76108-434)
Supplier:
Bioss
Description:
DHRS7 (dehydrogenase/reductase (SDR family) member 7), also known as SDR34C1, CGI-86 or retSDR4, is a 339 amino acid member of the SDR family. Like other members of the SDR family, DHRS7 contains a cofactor-binding Rossman-fold domain and is thought to catalyze the oxidation and reduction of a variety of substrates such as steroids and retinoids. DHRS7 exists as two alternatively spliced isoforms that are encoded by a gene located on human chromosome 14, which houses over 700 genes and comprises nearly 3.5% of the human genome. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease (AD). The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder ?-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction.
Catalog Number:
(76120-676)
Supplier:
Bioss
Description:
ANGEL2 is a 544 amino acid protein that belongs to the CCR4/nocturin family and exists as two alternatively spliced isoforms. The CCR4 family of proteins are 3_5_-deadenylases that function in the first step of the degradation of poly(A) mRNA. The CCR4 family most likely displays both RNA and ssDNA substrate preferences, thereby implicating a potential role in many regulatory processes. The ANGEL2 gene maps to human chromosome 1 (1q32.3), which is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. Chromosome 1 contains about 3,000 genes, and considering the great number of genes there are also a large number of diseases associated with it. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinson's disease, Gaucher disease and Usher syndrome are also associated with chromosome 1.
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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.
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