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(±)-2,2-Difluoro-1-methylcyclopropanecarboxylic+acid
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(±)-2,2-Difluoro-1-methylcyclopropanecarboxylic+acid
Catalog Number:
(102519-598)
Supplier:
Matrix Scientific
Description:
MF=C10H11F2NO3S MW=263.26 CAS=1254567-71-9 MDL=MFCD08443727 5G
Catalog Number:
(101777-904)
Supplier:
AOB CHEM USA
Description:
1-Chloro-2,3-difluoro-4-(hexyloxy)benzene ≥97%
Supplier:
AOB CHEM USA
Description:
(2,3-Difluoro-4-(methylthio)phenyl)methanol ≥97%
Supplier:
AOB CHEM USA
Description:
1,4-Difluoro-2-iodo-5-(methoxymethoxy)benzene ≥95%
Supplier:
AOB CHEM USA
Description:
(2,3-difluoro-6-(methylthio)phenyl)methanol ≥97%
Supplier:
AOB CHEM USA
Description:
2-Chloro-1,3-difluoro-4-(methoxymethyl)benzene ≥97%
Supplier:
AOB CHEM USA
Description:
4-Bromo-2,5-difluoro-N-methoxy-N-methylbenzamide ≥95%
Catalog Number:
(AAH26155-03)
Supplier:
AOB CHEM USA
Description:
1,3-Difluoro-2-(phenylmethoxy)benzene ≥97%
Supplier:
AOB CHEM USA
Description:
Ethyl 3,4-difluoro-2-methylbenzoate ≥95%
Catalog Number:
(76099-526)
Supplier:
Bioss
Description:
C9orf30 is a 275 amino acid protein that is expressed in brain and belongs to the UPF0439 family. The gene encoding C9orf30 maps to human chromosome 9q31.1. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Catalog Number:
(76099-518)
Supplier:
Bioss
Description:
C9orf23 (chromosome 9 open reading frame 23) is a 163 amino acid protein that belongs to the histone-like Alba family and is encoded by a gene that maps to human chromosome 9p13.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Supplier:
AOB CHEM USA
Description:
(2,3-Difluoro-4-iodo-6-methoxyphenyl)(methyl)sulfane ≥97%
Supplier:
AMBEED, INC
Description:
1-Bromo-2,4-difluoro-3-iodobenzene, Purity: 95%, CAS Number: 1208075-99-3, Appearance: Solid or liquid, Storage: Keep in dark place, Sealed in dry, Room Temperature, Size: 250mg
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 is still displayed and you need assistance, please call us at 1-800-932-5000.
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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