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Phenylacetaldehyde is an organic compound used in the synthesis of fragrances and polymers. [1] Phenylacetaldehyde is an aldehyde that consists of acetaldehyde bearing a phenyl substituent; the parent member of the phenylacetaldehyde class of compounds.
The check digit is found by taking the last digit times 1, the preceding digit times 2, the preceding digit times 3 etc., adding all these up and computing the sum modulo 10. For example, the CAS number of water is 7732-18-5: the checksum 5 is calculated as (8×1 + 1×2 + 2×3 + 3×4 + 7×5 + 7×6) = 105; 105 mod 10 = 5.
CAS number LaAlO 3: lanthanum aluminate: 71496–78–1 LaB 6: lanthanum boride: 12008–21–8 LaBr 3: lanthanum bromide: 13536–79–3 La(CHO 2) 3: lanthanum formate: 2081–11–0 LaC 2: lanthanum carbide: 12071–15–7 LaCl 3: lanthanum chloride: 10099–58–8 LaCl 3 •3H 2 O: lanthanum chloride trihydrate: 35564–84–2 LaCl 3 •7H 2 ...
CAS number; C 9 HF 17 O 2: perfluorononanoic acid: 375-95-1 C 9 H 2 Cl 6 O 3: chlorendic anhydride: 115-27-5 C 9 H 4 Cl 3 NO 2 S: folpet: 133-07-3 C 9 H 4 Cl 8 O: isobenzan: 297-78-9 C 9 H 4 O 5: trimellitic anhydride: 552-30-7 C 9 H 5 BrCrO 3: bromobenzenechromium tricarbonyl: 12082-02-9 C 9 H 5 CrFO 3: fluorobenzenechromium tricarbonyl: 12082 ...
The relationship between a CAS Registry Number and an INCI name is not always one-to-one. In some cases, more than one INCI name may have the same CAS number, or more than one CAS number may apply to an INCI name. For example, the CAS number 1245638-61-2 has the CA Index Name of 2-Propenoic acid, reaction products with pentaerythritol.
Phenyl glycidyl ether, is a liquid aromatic organic chemical in the glycidyl ether class of compounds. [2] It has the formula C 9 H 10 O 2.It has the CAS Registry Number 122-60-1 and the IUPAC name of 2-(phenoxymethyl)oxirane.
Triethylphosphite is prepared by treating phosphorus trichloride with ethanol in the presence of a base, typically a tertiary amine: [1] PCl 3 + 3 EtOH + 3 R 3 N → P(OEt) 3 + 3 R 3 NH + 3 Cl − In the absence of the base, the reaction of ethanol and phosphorus trichloride affords diethylphosphite ((EtO) 2 P(O)H).
Vinyltriethoxysilane and the related vinyltrimethoxysilane are used as monomers and comonomer for polymers such as ethylene-vinyltrimethoxysilane and ethylene-vinyl acetate-vinyltrimethoxysilane.